Canonical Allele Identifier: CA2333794519

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732823C= , CM000681.2:g.35732823C=	GRCh38
NC_000019.9:g.36223724C= , CM000681.1:g.36223724C=	GRCh37
NC_000019.8:g.40915564C=	NCBI36
NG_052906.1:g.19805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.580C=
ENST00000673918.2:c.6208C=	ENSP00000501283.1:p.Arg2070=
ENST00000674114.2:c.3815C=	ENSP00000501039.2:n.3815C=
ENST00000684977.1:c.1492C=	ENSP00000509384.1:p.Arg498=
ENST00000689544.1:n.1427C=
ENST00000691421.1:c.1495C=	ENSP00000508674.1:p.Arg499=
ENST00000691855.1:c.5816C=
ENST00000692961.1:c.6274C=	ENSP00000509289.1:p.Arg2092=
ENST00000693677.1:c.704+494C=	ENSP00000509779.1:n.704+494C=
ENST00000420124.4:c.6274C= MANE Select	ENSP00000398837.2:p.Arg2092=
ENST00000673918.1:c.6208C=	ENSP00000501283.1:p.Arg2070=
ENST00000674114.1:c.3596C=
ENST00000420124.2:c.6274C=	ENSP00000398837.1:p.Arg2092=
NM_014727.2:c.6274C=	NP_055542.1:p.Arg2092=
XM_011527561.1:c.6208C=	XP_011525863.1:p.Arg2070=
XM_011527562.1:c.6274C=	XP_011525864.1:p.Arg2092=
XM_011527563.1:c.5998C=	XP_011525865.1:p.Arg2000=
XM_011527561.2:c.5710C=	XP_011525863.2:p.Arg1904=
XM_011527562.2:c.6274C=	XP_011525864.1:p.Arg2092=
XM_017027544.1:c.6274C=	XP_016883033.1:p.Arg2092=
XM_017027545.1:c.5710C=	XP_016883034.1:p.Arg1904=
XM_017027546.1:c.3238C=	XP_016883035.1:p.Arg1080=
NM_014727.3:c.6274C= MANE Select	NP_055542.1:p.Arg2092=