Canonical Allele Identifier: CA3710762
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41562313
ExAC: 6:31239058 A / G
gnomAD v2: 6-31239058-A-G
gnomAD v3: 6-31271281-A-G
gnomAD v4: 6-31271281-A-G
MyVariant Identifiers: chr6:g.31239058A>G (hg19) chr6:g.31271281A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271281A>G , CM000668.2:g.31271281A>G GRCh38
NC_000006.11:g.31239058A>G , CM000668.1:g.31239058A>G GRCh37
NC_000006.10:g.31347037A>G NCBI36
NG_029422.2:g.5851T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.411T>C MANE Select ENSP00000365402.5:p.Tyr137=
ENST00000376228.9:c.411T>C ENSP00000365402.5:p.Tyr137=
ENST00000376237.8:c.394T>C ENSP00000365412.4:p.Ter132Arg
ENST00000383329.7:c.411T>C ENSP00000372819.3:p.Tyr137=
ENST00000415537.1:c.409T>C
ENST00000484378.1:n.680T>C
ENST00000487245.5:n.770T>C
ENST00000495835.1:n.600T>C
NM_002117.5:c.411T>C NP_002108.4:p.Tyr137=
NM_002117.6:c.411T>C MANE Select NP_002108.4:p.Tyr137=
Search 100 bp 5'
Search 100 bp 3'