Canonical Allele Identifier: CA1619723871

Gene: HLA-DQB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32757416A= , CM000668.2:g.32757416A=	GRCh38
NC_000006.11:g.32725193A= , CM000668.1:g.32725193A=	GRCh37
NC_000006.10:g.32833171A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437316.7:c.758-112T= MANE Select	ENSP00000396330.2:n.758-112T=
ENST00000411527.5:c.647-112T=	ENSP00000390431.1:n.647-112T=
ENST00000427449.1:c.643-950T=
ENST00000435145.6:c.758-112T=	ENSP00000410512.2:n.758-112T=
ENST00000437316.6:c.758-112T=	ENSP00000396330.2:n.758-112T=
NM_001198858.1:c.647-112T=	NP_001185787.1:n.647-112T=
NM_001300790.1:c.758-112T=	NP_001287719.1:n.758-112T=
XM_005249051.3:c.758-112T=	XP_005249108.1:n.758-112T=
XM_011514560.1:c.757+357T=	XP_011512862.1:n.757+357T=
XM_011514561.1:c.647-950T=	XP_011512863.1:n.647-950T=
XM_005249051.4:c.758-112T=	XP_005249108.1:n.758-112T=
XM_011514560.2:c.757+357T=	XP_011512862.1:n.757+357T=
XM_011514561.3:c.647-950T=	XP_011512863.1:n.647-950T=
NM_001300790.2:c.758-112T= MANE Select	NP_001287719.1:n.758-112T=
NM_001198858.2:c.647-112T=	NP_001185787.1:n.647-112T=