Canonical Allele Identifier: CA2333794394

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732604G= , CM000681.2:g.35732604G=	GRCh38
NC_000019.9:g.36223505G= , CM000681.1:g.36223505G=	GRCh37
NC_000019.8:g.40915345G=	NCBI36
NG_052906.1:g.19586G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.361G=
ENST00000673918.2:c.5989G=	ENSP00000501283.1:p.Gly1997=
ENST00000674114.2:c.3596G=	ENSP00000501039.2:n.3596G=
ENST00000684977.1:c.1273G=	ENSP00000509384.1:p.Gly425=
ENST00000689544.1:n.1208G=
ENST00000691421.1:c.1276G=	ENSP00000508674.1:p.Gly426=
ENST00000691855.1:c.5597G=
ENST00000692961.1:c.6055G=	ENSP00000509289.1:p.Gly2019=
ENST00000693677.1:c.704+275G=	ENSP00000509779.1:n.704+275G=
ENST00000420124.4:c.6055G= MANE Select	ENSP00000398837.2:p.Gly2019=
ENST00000673918.1:c.5989G=	ENSP00000501283.1:p.Gly1997=
ENST00000674114.1:c.3377G=
ENST00000420124.2:c.6055G=	ENSP00000398837.1:p.Gly2019=
NM_014727.2:c.6055G=	NP_055542.1:p.Gly2019=
XM_011527561.1:c.5989G=	XP_011525863.1:p.Gly1997=
XM_011527562.1:c.6055G=	XP_011525864.1:p.Gly2019=
XM_011527563.1:c.5779G=	XP_011525865.1:p.Gly1927=
XM_011527561.2:c.5491G=	XP_011525863.2:p.Gly1831=
XM_011527562.2:c.6055G=	XP_011525864.1:p.Gly2019=
XM_017027544.1:c.6055G=	XP_016883033.1:p.Gly2019=
XM_017027545.1:c.5491G=	XP_016883034.1:p.Gly1831=
XM_017027546.1:c.3019G=	XP_016883035.1:p.Gly1007=
NM_014727.3:c.6055G= MANE Select	NP_055542.1:p.Gly2019=