Canonical Allele Identifier: CA566689014

Gene: HLA-C

Linked Data

• dbSNP Id: rs1174978708
• gnomAD v2: 6-31239229-A-C
• gnomAD v3: 6-31271452-A-C
• gnomAD v4: 6-31271452-A-C
• MyVariant Identifiers: chr6:g.31239229A>C (hg19) ; chr6:g.31271452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271452A>C , CM000668.2:g.31271452A>C	GRCh38
NC_000006.11:g.31239229A>C , CM000668.1:g.31239229A>C	GRCh37
NC_000006.10:g.31347208A>C	NCBI36
NG_029422.2:g.5680T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-104T>G MANE Select	ENSP00000365402.5:n.344-104T>G
ENST00000376228.9:c.344-104T>G	ENSP00000365402.5:n.344-104T>G
ENST00000376237.8:c.344-121T>G	ENSP00000365412.4:n.344-121T>G
ENST00000383329.7:c.344-104T>G	ENSP00000372819.3:n.344-104T>G
ENST00000415537.1:c.342-104T>G
ENST00000484378.1:n.509T>G
ENST00000487245.5:n.599T>G
ENST00000495835.1:n.533-104T>G
NM_002117.5:c.344-104T>G	NP_002108.4:n.344-104T>G
NM_002117.6:c.344-104T>G MANE Select	NP_002108.4:n.344-104T>G