Canonical Allele Identifier: CA1619077116

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761079414

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268822dup , CM000668.2:g.31268822dup	GRCh38
NC_000006.11:g.31236599dup , CM000668.1:g.31236599dup	GRCh37
NC_000006.10:g.31344578dup	NCBI36
NG_029422.2:g.8310dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*347dup MANE Select	ENSP00000365402.5:n.*347dup
ENST00000376228.9:c.*347dup	ENSP00000365402.5:n.*347dup
ENST00000376237.8:c.*1035dup	ENSP00000365412.4:n.*1035dup
ENST00000383329.7:c.*347dup	ENSP00000372819.3:n.*347dup
ENST00000466892.5:n.681dup
ENST00000470363.5:n.1206dup
ENST00000487245.5:n.1807dup
NM_002117.5:c.*347dup	NP_002108.4:n.*347dup
NM_002117.6:c.*347dup MANE Select	NP_002108.4:n.*347dup