Canonical Allele Identifier: CA3710802

Gene: HLA-C

Linked Data

• dbSNP Id: rs756406145
• ExAC: 6:31239127 T / A
• gnomAD v2: 6-31239127-T-A
• gnomAD v4: 6-31271350-T-A
• MyVariant Identifiers: chr6:g.31239127T>A (hg19) ; chr6:g.31271350T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271350T>A , CM000668.2:g.31271350T>A	GRCh38
NC_000006.11:g.31239127T>A , CM000668.1:g.31239127T>A	GRCh37
NC_000006.10:g.31347106T>A	NCBI36
NG_029422.2:g.5782A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-2A>T MANE Select	ENSP00000365402.5:n.344-2A>T
ENST00000376228.9:c.344-2A>T	ENSP00000365402.5:n.344-2A>T
ENST00000376237.8:c.344-19A>T	ENSP00000365412.4:n.344-19A>T
ENST00000383329.7:c.344-2A>T	ENSP00000372819.3:n.344-2A>T
ENST00000415537.1:c.342-2A>T
ENST00000484378.1:n.611A>T
ENST00000487245.5:n.701A>T
ENST00000495835.1:n.533-2A>T
NM_002117.5:c.344-2A>T	NP_002108.4:n.344-2A>T
NM_002117.6:c.344-2A>T MANE Select	NP_002108.4:n.344-2A>T