Canonical Allele Identifier: CA1619080573

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761337144
• gnomAD v4: 6-31271374-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271375dup , CM000668.2:g.31271375dup	GRCh38
NC_000006.11:g.31239152dup , CM000668.1:g.31239152dup	GRCh37
NC_000006.10:g.31347131dup	NCBI36
NG_029422.2:g.5757dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-27dup MANE Select	ENSP00000365402.5:n.344-27dup
ENST00000376228.9:c.344-27dup	ENSP00000365402.5:n.344-27dup
ENST00000376237.8:c.344-44dup	ENSP00000365412.4:n.344-44dup
ENST00000383329.7:c.344-27dup	ENSP00000372819.3:n.344-27dup
ENST00000415537.1:c.342-27dup
ENST00000484378.1:n.586dup
ENST00000487245.5:n.676dup
ENST00000495835.1:n.533-27dup
NM_002117.5:c.344-27dup	NP_002108.4:n.344-27dup
NM_002117.6:c.344-27dup MANE Select	NP_002108.4:n.344-27dup