Canonical Allele Identifier: CA2333794342

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732481G= , CM000681.2:g.35732481G=	GRCh38
NC_000019.9:g.36223382G= , CM000681.1:g.36223382G=	GRCh37
NC_000019.8:g.40915222G=	NCBI36
NG_052906.1:g.19463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.238G=
ENST00000673918.2:c.5866G=	ENSP00000501283.1:p.Glu1956=
ENST00000674114.2:c.3473G=	ENSP00000501039.2:n.3473G=
ENST00000684977.1:c.1150G=	ENSP00000509384.1:p.Glu384=
ENST00000689544.1:n.1085G=
ENST00000691421.1:c.1153G=	ENSP00000508674.1:p.Glu385=
ENST00000691855.1:c.5474G=
ENST00000692961.1:c.5932G=	ENSP00000509289.1:p.Glu1978=
ENST00000693677.1:c.704+152G=	ENSP00000509779.1:n.704+152G=
ENST00000420124.4:c.5932G= MANE Select	ENSP00000398837.2:p.Glu1978=
ENST00000673918.1:c.5866G=	ENSP00000501283.1:p.Glu1956=
ENST00000674114.1:c.3254G=
ENST00000420124.2:c.5932G=	ENSP00000398837.1:p.Glu1978=
NM_014727.2:c.5932G=	NP_055542.1:p.Glu1978=
XM_011527561.1:c.5866G=	XP_011525863.1:p.Glu1956=
XM_011527562.1:c.5932G=	XP_011525864.1:p.Glu1978=
XM_011527563.1:c.5656G=	XP_011525865.1:p.Glu1886=
XM_011527561.2:c.5368G=	XP_011525863.2:p.Glu1790=
XM_011527562.2:c.5932G=	XP_011525864.1:p.Glu1978=
XM_017027544.1:c.5932G=	XP_016883033.1:p.Glu1978=
XM_017027545.1:c.5368G=	XP_016883034.1:p.Glu1790=
XM_017027546.1:c.2896G=	XP_016883035.1:p.Glu966=
NM_014727.3:c.5932G= MANE Select	NP_055542.1:p.Glu1978=