Canonical Allele Identifier: CA1087449564
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269269-A-T
gnomAD v4: 6-31269269-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269269A>T , CM000668.2:g.31269269A>T GRCh38
NC_000006.11:g.31237046A>T , CM000668.1:g.31237046A>T GRCh37
NC_000006.10:g.31345025A>T NCBI36
NG_029422.2:g.7863T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1096+69T>A MANE Select ENSP00000365402.5:n.1096+69T>A
ENST00000376228.9:c.1096+69T>A ENSP00000365402.5:n.1096+69T>A
ENST00000376237.8:c.*683+69T>A ENSP00000365412.4:n.*683+69T>A
ENST00000383329.7:c.1114+69T>A ENSP00000372819.3:n.1114+69T>A
ENST00000466892.5:n.329+69T>A
ENST00000470363.5:n.854+69T>A
ENST00000487245.5:n.1455+69T>A
NM_002117.5:c.1096+69T>A NP_002108.4:n.1096+69T>A
NM_002117.6:c.1096+69T>A MANE Select NP_002108.4:n.1096+69T>A
Search 100 bp 5'
Search 100 bp 3'