Canonical Allele Identifier: CA2333794637

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733066C= , CM000681.2:g.35733066C=	GRCh38
NC_000019.9:g.36223967C= , CM000681.1:g.36223967C=	GRCh37
NC_000019.8:g.40915807C=	NCBI36
NG_052906.1:g.20048C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.823C=
ENST00000673918.2:c.6451C=	ENSP00000501283.1:p.Arg2151=
ENST00000674114.2:c.4058C=	ENSP00000501039.2:n.4058C=
ENST00000684977.1:c.1735C=	ENSP00000509384.1:p.Arg579=
ENST00000689544.1:n.1670C=
ENST00000691421.1:c.1738C=	ENSP00000508674.1:p.Arg580=
ENST00000691855.1:c.6059C=
ENST00000692961.1:c.6517C=	ENSP00000509289.1:p.Arg2173=
ENST00000693677.1:c.705-531C=	ENSP00000509779.1:n.705-531C=
ENST00000420124.4:c.6517C= MANE Select	ENSP00000398837.2:p.Arg2173=
ENST00000673918.1:c.6451C=	ENSP00000501283.1:p.Arg2151=
ENST00000674114.1:c.3839C=
ENST00000420124.2:c.6517C=	ENSP00000398837.1:p.Arg2173=
NM_014727.2:c.6517C=	NP_055542.1:p.Arg2173=
XM_011527561.1:c.6451C=	XP_011525863.1:p.Arg2151=
XM_011527562.1:c.6517C=	XP_011525864.1:p.Arg2173=
XM_011527563.1:c.6241C=	XP_011525865.1:p.Arg2081=
XM_011527561.2:c.5953C=	XP_011525863.2:p.Arg1985=
XM_011527562.2:c.6517C=	XP_011525864.1:p.Arg2173=
XM_017027544.1:c.6517C=	XP_016883033.1:p.Arg2173=
XM_017027545.1:c.5953C=	XP_016883034.1:p.Arg1985=
XM_017027546.1:c.3481C=	XP_016883035.1:p.Arg1161=
NM_014727.3:c.6517C= MANE Select	NP_055542.1:p.Arg2173=