Canonical Allele Identifier: CA2333794506

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732787G= , CM000681.2:g.35732787G=	GRCh38
NC_000019.9:g.36223688G= , CM000681.1:g.36223688G=	GRCh37
NC_000019.8:g.40915528G=	NCBI36
NG_052906.1:g.19769G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.544G=
ENST00000673918.2:c.6172G=	ENSP00000501283.1:p.Gly2058=
ENST00000674114.2:c.3779G=	ENSP00000501039.2:n.3779G=
ENST00000684977.1:c.1456G=	ENSP00000509384.1:p.Gly486=
ENST00000689544.1:n.1391G=
ENST00000691421.1:c.1459G=	ENSP00000508674.1:p.Gly487=
ENST00000691855.1:c.5780G=
ENST00000692961.1:c.6238G=	ENSP00000509289.1:p.Gly2080=
ENST00000693677.1:c.704+458G=	ENSP00000509779.1:n.704+458G=
ENST00000420124.4:c.6238G= MANE Select	ENSP00000398837.2:p.Gly2080=
ENST00000673918.1:c.6172G=	ENSP00000501283.1:p.Gly2058=
ENST00000674114.1:c.3560G=
ENST00000420124.2:c.6238G=	ENSP00000398837.1:p.Gly2080=
NM_014727.2:c.6238G=	NP_055542.1:p.Gly2080=
XM_011527561.1:c.6172G=	XP_011525863.1:p.Gly2058=
XM_011527562.1:c.6238G=	XP_011525864.1:p.Gly2080=
XM_011527563.1:c.5962G=	XP_011525865.1:p.Gly1988=
XM_011527561.2:c.5674G=	XP_011525863.2:p.Gly1892=
XM_011527562.2:c.6238G=	XP_011525864.1:p.Gly2080=
XM_017027544.1:c.6238G=	XP_016883033.1:p.Gly2080=
XM_017027545.1:c.5674G=	XP_016883034.1:p.Gly1892=
XM_017027546.1:c.3202G=	XP_016883035.1:p.Gly1068=
NM_014727.3:c.6238G= MANE Select	NP_055542.1:p.Gly2080=