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Human Genome Region MHC

Assembly:
GRCh37.p13
Location:
chr6:28,477,797-33,448,354
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL000250.1 NT_167244.1 ALT 4,622,290 18,094 24,715
GL000251.1 NT_113891.2 ALT 4,795,371 30,205 98,149
GL000252.1 NT_167245.1 ALT 4,610,396 23,687 119,717
GL000253.1 NT_167246.1 ALT 4,683,263 51,809 200,051
GL000254.1 NT_167247.1 ALT 4,833,398 18,673 82,470
GL000255.1 NT_167248.1 ALT 4,611,984 33,042 77,205
GL000256.1 NT_167249.1 ALT 4,928,567 26,019 212,264
JH636057.1 NW_003871063.1 FIX 200,195 1,470 55,978
           

MHC -- chr6 (NC_000006.11):28,477,797-33,448,354