Canonical Allele Identifier: CA1087427283

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761343134
• gnomAD v3: 6-31271415-T-C
• gnomAD v4: 6-31271415-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271415T>C , CM000668.2:g.31271415T>C	GRCh38
NC_000006.11:g.31239192T>C , CM000668.1:g.31239192T>C	GRCh37
NC_000006.10:g.31347171T>C	NCBI36
NG_029422.2:g.5717A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-67A>G MANE Select	ENSP00000365402.5:n.344-67A>G
ENST00000376228.9:c.344-67A>G	ENSP00000365402.5:n.344-67A>G
ENST00000376237.8:c.344-84A>G	ENSP00000365412.4:n.344-84A>G
ENST00000383329.7:c.344-67A>G	ENSP00000372819.3:n.344-67A>G
ENST00000415537.1:c.342-67A>G
ENST00000484378.1:n.546A>G
ENST00000487245.5:n.636A>G
ENST00000495835.1:n.533-67A>G
NM_002117.5:c.344-67A>G	NP_002108.4:n.344-67A>G
NM_002117.6:c.344-67A>G MANE Select	NP_002108.4:n.344-67A>G