Canonical Allele Identifier: CA1619724651

Gene: HLA-DQB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32759026C= , CM000668.2:g.32759026C=	GRCh38
NC_000006.11:g.32726803C= , CM000668.1:g.32726803C=	GRCh37
NC_000006.10:g.32834781C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001300790.2:c.470G= MANE Select	NP_001287719.1:p.Arg157=
ENST00000437316.7:c.470G= MANE Select	ENSP00000396330.2:p.Arg157=
NM_001198858.1:c.470G=	NP_001185787.1:p.Arg157=
NM_001198858.2:c.470G=	NP_001185787.1:p.Arg157=
NM_001300790.1:c.470G=	NP_001287719.1:p.Arg157=
ENST00000411527.5:c.470G=	ENSP00000390431.1:p.Arg157=
ENST00000427449.1:c.466G=
ENST00000435145.6:c.470G=	ENSP00000410512.2:p.Arg157=
ENST00000437316.6:c.470G=	ENSP00000396330.2:p.Arg157=
XM_005249051.3:c.470G=	XP_005249108.1:p.Arg157=
XM_005249051.4:c.470G=	XP_005249108.1:p.Arg157=
XM_011514560.1:c.470G=	XP_011512862.1:p.Arg157=
XM_011514560.2:c.470G=	XP_011512862.1:p.Arg157=
XM_011514561.1:c.470G=	XP_011512863.1:p.Arg157=
XM_011514561.3:c.470G=	XP_011512863.1:p.Arg157=