Canonical Allele Identifier: CA566689007

Gene: HLA-C

Linked Data

• dbSNP Id: rs762175456
• gnomAD v2: 6-31239173-C-A
• gnomAD v3: 6-31271396-C-A
• gnomAD v4: 6-31271396-C-A
• MyVariant Identifiers: chr6:g.31239173C>A (hg19) ; chr6:g.31271396C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271396C>A , CM000668.2:g.31271396C>A	GRCh38
NC_000006.11:g.31239173C>A , CM000668.1:g.31239173C>A	GRCh37
NC_000006.10:g.31347152C>A	NCBI36
NG_029422.2:g.5736G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-48G>T MANE Select	ENSP00000365402.5:n.344-48G>T
ENST00000376228.9:c.344-48G>T	ENSP00000365402.5:n.344-48G>T
ENST00000376237.8:c.344-65G>T	ENSP00000365412.4:n.344-65G>T
ENST00000383329.7:c.344-48G>T	ENSP00000372819.3:n.344-48G>T
ENST00000415537.1:c.342-48G>T
ENST00000484378.1:n.565G>T
ENST00000487245.5:n.655G>T
ENST00000495835.1:n.533-48G>T
NM_002117.5:c.344-48G>T	NP_002108.4:n.344-48G>T
NM_002117.6:c.344-48G>T MANE Select	NP_002108.4:n.344-48G>T