Canonical Allele Identifier: CA363319262

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269359-C-G
• MyVariant Identifiers: chr6:g.31237136C>G (hg19) ; chr6:g.31269359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269359C>G , CM000668.2:g.31269359C>G	GRCh38
NC_000006.11:g.31237136C>G , CM000668.1:g.31237136C>G	GRCh37
NC_000006.10:g.31345115C>G	NCBI36
NG_029422.2:g.7773G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1075G>C MANE Select	ENSP00000365402.5:p.Glu359Gln
ENST00000376228.9:c.1075G>C	ENSP00000365402.5:p.Glu359Gln
ENST00000376237.8:c.*662G>C	ENSP00000365412.4:n.*662G>C
ENST00000383329.7:c.1093G>C	ENSP00000372819.3:p.Glu365Gln
ENST00000466892.5:n.308G>C
ENST00000470363.5:n.833G>C
ENST00000487245.5:n.1434G>C
NM_002117.5:c.1075G>C	NP_002108.4:p.Glu359Gln
NM_002117.6:c.1075G>C MANE Select	NP_002108.4:p.Glu359Gln