Canonical Allele Identifier: CA2333794573

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732947A= , CM000681.2:g.35732947A=	GRCh38
NC_000019.9:g.36223848A= , CM000681.1:g.36223848A=	GRCh37
NC_000019.8:g.40915688A=	NCBI36
NG_052906.1:g.19929A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.704A=
ENST00000673918.2:c.6332A=	ENSP00000501283.1:p.Glu2111=
ENST00000674114.2:c.3939A=	ENSP00000501039.2:n.3939A=
ENST00000684977.1:c.1616A=	ENSP00000509384.1:p.Glu539=
ENST00000689544.1:n.1551A=
ENST00000691421.1:c.1619A=	ENSP00000508674.1:p.Glu540=
ENST00000691855.1:c.5940A=
ENST00000692961.1:c.6398A=	ENSP00000509289.1:p.Glu2133=
ENST00000693677.1:c.704+618A=	ENSP00000509779.1:n.704+618A=
ENST00000420124.4:c.6398A= MANE Select	ENSP00000398837.2:p.Glu2133=
ENST00000673918.1:c.6332A=	ENSP00000501283.1:p.Glu2111=
ENST00000674114.1:c.3720A=
ENST00000420124.2:c.6398A=	ENSP00000398837.1:p.Glu2133=
NM_014727.2:c.6398A=	NP_055542.1:p.Glu2133=
XM_011527561.1:c.6332A=	XP_011525863.1:p.Glu2111=
XM_011527562.1:c.6398A=	XP_011525864.1:p.Glu2133=
XM_011527563.1:c.6122A=	XP_011525865.1:p.Glu2041=
XM_011527561.2:c.5834A=	XP_011525863.2:p.Glu1945=
XM_011527562.2:c.6398A=	XP_011525864.1:p.Glu2133=
XM_017027544.1:c.6398A=	XP_016883033.1:p.Glu2133=
XM_017027545.1:c.5834A=	XP_016883034.1:p.Glu1945=
XM_017027546.1:c.3362A=	XP_016883035.1:p.Glu1121=
NM_014727.3:c.6398A= MANE Select	NP_055542.1:p.Glu2133=