Canonical Allele Identifier: CA449790230

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761337515
• gnomAD v3: 6-31271378-C-A
• gnomAD v4: 6-31271378-C-A
• MyVariant Identifiers: chr6:g.31239155C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271378C>A , CM000668.2:g.31271378C>A	GRCh38
NC_000006.11:g.31239155C>A , CM000668.1:g.31239155C>A	GRCh37
NC_000006.10:g.31347134C>A	NCBI36
NG_029422.2:g.5754G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-30G>T MANE Select	ENSP00000365402.5:n.344-30G>T
ENST00000376228.9:c.344-30G>T	ENSP00000365402.5:n.344-30G>T
ENST00000376237.8:c.344-47G>T	ENSP00000365412.4:n.344-47G>T
ENST00000383329.7:c.344-30G>T	ENSP00000372819.3:n.344-30G>T
ENST00000415537.1:c.342-30G>T
ENST00000484378.1:n.583G>T
ENST00000487245.5:n.673G>T
ENST00000495835.1:n.533-30G>T
NM_002117.5:c.344-30G>T	NP_002108.4:n.344-30G>T
NM_002117.6:c.344-30G>T MANE Select	NP_002108.4:n.344-30G>T