Canonical Allele Identifier: CA449790329

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761210714
• gnomAD v4: 6-31270286-C-T
• MyVariant Identifiers: chr6:g.31238063C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270286C>T , CM000668.2:g.31270286C>T	GRCh38
NC_000006.11:g.31238063C>T , CM000668.1:g.31238063C>T	GRCh37
NC_000006.10:g.31346042C>T	NCBI36
NG_029422.2:g.6846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.819G>A MANE Select	ENSP00000365402.5:p.Val273=
ENST00000376228.9:c.819G>A	ENSP00000365402.5:p.Val273=
ENST00000376237.8:c.*406G>A	ENSP00000365412.4:n.*406G>A
ENST00000383329.7:c.819G>A	ENSP00000372819.3:p.Val273=
ENST00000415537.1:c.710G>A
ENST00000470363.5:n.137G>A
ENST00000487245.5:n.1178G>A
ENST00000495835.1:n.1008G>A
NM_002117.5:c.819G>A	NP_002108.4:p.Val273=
NM_002117.6:c.819G>A MANE Select	NP_002108.4:p.Val273=