Canonical Allele Identifier: CA2333794517

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732815G= , CM000681.2:g.35732815G=	GRCh38
NC_000019.9:g.36223716G= , CM000681.1:g.36223716G=	GRCh37
NC_000019.8:g.40915556G=	NCBI36
NG_052906.1:g.19797G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.572G=
ENST00000673918.2:c.6200G=	ENSP00000501283.1:p.Gly2067=
ENST00000674114.2:c.3807G=	ENSP00000501039.2:n.3807G=
ENST00000684977.1:c.1484G=	ENSP00000509384.1:p.Gly495=
ENST00000689544.1:n.1419G=
ENST00000691421.1:c.1487G=	ENSP00000508674.1:p.Gly496=
ENST00000691855.1:c.5808G=
ENST00000692961.1:c.6266G=	ENSP00000509289.1:p.Gly2089=
ENST00000693677.1:c.704+486G=	ENSP00000509779.1:n.704+486G=
ENST00000420124.4:c.6266G= MANE Select	ENSP00000398837.2:p.Gly2089=
ENST00000673918.1:c.6200G=	ENSP00000501283.1:p.Gly2067=
ENST00000674114.1:c.3588G=
ENST00000420124.2:c.6266G=	ENSP00000398837.1:p.Gly2089=
NM_014727.2:c.6266G=	NP_055542.1:p.Gly2089=
XM_011527561.1:c.6200G=	XP_011525863.1:p.Gly2067=
XM_011527562.1:c.6266G=	XP_011525864.1:p.Gly2089=
XM_011527563.1:c.5990G=	XP_011525865.1:p.Gly1997=
XM_011527561.2:c.5702G=	XP_011525863.2:p.Gly1901=
XM_011527562.2:c.6266G=	XP_011525864.1:p.Gly2089=
XM_017027544.1:c.6266G=	XP_016883033.1:p.Gly2089=
XM_017027545.1:c.5702G=	XP_016883034.1:p.Gly1901=
XM_017027546.1:c.3230G=	XP_016883035.1:p.Gly1077=
NM_014727.3:c.6266G= MANE Select	NP_055542.1:p.Gly2089=