Canonical Allele Identifier: CA363319768

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270049-A-T
• MyVariant Identifiers: chr6:g.31237826A>T (hg19) ; chr6:g.31270049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270049A>T , CM000668.2:g.31270049A>T	GRCh38
NC_000006.11:g.31237826A>T , CM000668.1:g.31237826A>T	GRCh37
NC_000006.10:g.31345805A>T	NCBI36
NG_029422.2:g.7083T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.932T>A MANE Select	ENSP00000365402.5:p.Ile311Asn
ENST00000376228.9:c.932T>A	ENSP00000365402.5:p.Ile311Asn
ENST00000376237.8:c.*519T>A	ENSP00000365412.4:n.*519T>A
ENST00000383329.7:c.932T>A	ENSP00000372819.3:p.Ile311Asn
ENST00000470363.5:n.250T>A
ENST00000487245.5:n.1291T>A
NM_002117.5:c.932T>A	NP_002108.4:p.Ile311Asn
NM_002117.6:c.932T>A MANE Select	NP_002108.4:p.Ile311Asn