Canonical Allele Identifier: CA136861187
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs764717839
gnomAD v2: 6-31236784-G-A
gnomAD v3: 6-31269007-G-A
gnomAD v4: 6-31269007-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269007G>A , CM000668.2:g.31269007G>A GRCh38
NC_000006.11:g.31236784G>A , CM000668.1:g.31236784G>A GRCh37
NC_000006.10:g.31344763G>A NCBI36
NG_029422.2:g.8125C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*162C>T MANE Select ENSP00000365402.5:n.*162C>T
ENST00000376228.9:c.*162C>T ENSP00000365402.5:n.*162C>T
ENST00000376237.8:c.*850C>T ENSP00000365412.4:n.*850C>T
ENST00000383329.7:c.*162C>T ENSP00000372819.3:n.*162C>T
ENST00000466892.5:n.496C>T
ENST00000470363.5:n.1021C>T
ENST00000487245.5:n.1622C>T
NM_002117.5:c.*162C>T NP_002108.4:n.*162C>T
NM_002117.6:c.*162C>T MANE Select NP_002108.4:n.*162C>T