Canonical Allele Identifier: CA2333794393

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732602G= , CM000681.2:g.35732602G=	GRCh38
NC_000019.9:g.36223503G= , CM000681.1:g.36223503G=	GRCh37
NC_000019.8:g.40915343G=	NCBI36
NG_052906.1:g.19584G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.359G=
ENST00000673918.2:c.5987G=	ENSP00000501283.1:p.Gly1996=
ENST00000674114.2:c.3594G=	ENSP00000501039.2:n.3594G=
ENST00000684977.1:c.1271G=	ENSP00000509384.1:p.Gly424=
ENST00000689544.1:n.1206G=
ENST00000691421.1:c.1274G=	ENSP00000508674.1:p.Gly425=
ENST00000691855.1:c.5595G=
ENST00000692961.1:c.6053G=	ENSP00000509289.1:p.Gly2018=
ENST00000693677.1:c.704+273G=	ENSP00000509779.1:n.704+273G=
ENST00000420124.4:c.6053G= MANE Select	ENSP00000398837.2:p.Gly2018=
ENST00000673918.1:c.5987G=	ENSP00000501283.1:p.Gly1996=
ENST00000674114.1:c.3375G=
ENST00000420124.2:c.6053G=	ENSP00000398837.1:p.Gly2018=
NM_014727.2:c.6053G=	NP_055542.1:p.Gly2018=
XM_011527561.1:c.5987G=	XP_011525863.1:p.Gly1996=
XM_011527562.1:c.6053G=	XP_011525864.1:p.Gly2018=
XM_011527563.1:c.5777G=	XP_011525865.1:p.Gly1926=
XM_011527561.2:c.5489G=	XP_011525863.2:p.Gly1830=
XM_011527562.2:c.6053G=	XP_011525864.1:p.Gly2018=
XM_017027544.1:c.6053G=	XP_016883033.1:p.Gly2018=
XM_017027545.1:c.5489G=	XP_016883034.1:p.Gly1830=
XM_017027546.1:c.3017G=	XP_016883035.1:p.Gly1006=
NM_014727.3:c.6053G= MANE Select	NP_055542.1:p.Gly2018=