Canonical Allele Identifier: CA363318890

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31269173-G-T
• gnomAD v4: 6-31269173-G-T
• MyVariant Identifiers: chr6:g.31236950G>T (hg19) ; chr6:g.31269173G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269173G>T , CM000668.2:g.31269173G>T	GRCh38
NC_000006.11:g.31236950G>T , CM000668.1:g.31236950G>T	GRCh37
NC_000006.10:g.31344929G>T	NCBI36
NG_029422.2:g.7959C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1097C>A MANE Select	ENSP00000365402.5:p.Ala366Asp
ENST00000376228.9:c.1097C>A	ENSP00000365402.5:p.Ala366Asp
ENST00000376237.8:c.*684C>A	ENSP00000365412.4:n.*684C>A
ENST00000383329.7:c.1115C>A	ENSP00000372819.3:p.Ala372Asp
ENST00000466892.5:n.330C>A
ENST00000470363.5:n.855C>A
ENST00000487245.5:n.1456C>A
NM_002117.5:c.1097C>A	NP_002108.4:p.Ala366Asp
NM_002117.6:c.1097C>A MANE Select	NP_002108.4:p.Ala366Asp