Canonical Allele Identifier: CA363326624

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271274-A-T
• MyVariant Identifiers: chr6:g.31239051A>T (hg19) ; chr6:g.31271274A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271274A>T , CM000668.2:g.31271274A>T	GRCh38
NC_000006.11:g.31239051A>T , CM000668.1:g.31239051A>T	GRCh37
NC_000006.10:g.31347030A>T	NCBI36
NG_029422.2:g.5858T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.418T>A MANE Select	ENSP00000365402.5:p.Ser140Thr
ENST00000376228.9:c.418T>A	ENSP00000365402.5:p.Ser140Thr
ENST00000376237.8:c.*5T>A	ENSP00000365412.4:n.*5T>A
ENST00000383329.7:c.418T>A	ENSP00000372819.3:p.Ser140Thr
ENST00000415537.1:c.416T>A
ENST00000484378.1:n.687T>A
ENST00000487245.5:n.777T>A
ENST00000495835.1:n.607T>A
NM_002117.5:c.418T>A	NP_002108.4:p.Ser140Thr
NM_002117.6:c.418T>A MANE Select	NP_002108.4:p.Ser140Thr