Canonical Allele Identifier: CA3710763
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41555122
ExAC: 6:31239059 T / C
gnomAD v2: 6-31239059-T-C
gnomAD v3: 6-31271282-T-C
gnomAD v4: 6-31271282-T-C
MyVariant Identifiers: chr6:g.31239059T>C (hg19) chr6:g.31271282T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271282T>C , CM000668.2:g.31271282T>C GRCh38
NC_000006.11:g.31239059T>C , CM000668.1:g.31239059T>C GRCh37
NC_000006.10:g.31347038T>C NCBI36
NG_029422.2:g.5850A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.410A>G MANE Select ENSP00000365402.5:p.Tyr137Cys
ENST00000376228.9:c.410A>G ENSP00000365402.5:p.Tyr137Cys
ENST00000376237.8:c.393A>G ENSP00000365412.4:p.Val131=
ENST00000383329.7:c.410A>G ENSP00000372819.3:p.Tyr137Cys
ENST00000415537.1:c.408A>G
ENST00000484378.1:n.679A>G
ENST00000487245.5:n.769A>G
ENST00000495835.1:n.599A>G
NM_002117.5:c.410A>G NP_002108.4:p.Tyr137Cys
NM_002117.6:c.410A>G MANE Select NP_002108.4:p.Tyr137Cys
Search 100 bp 5'
Search 100 bp 3'