Canonical Allele Identifier: CA2333795035

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733773G= , CM000681.2:g.35733773G=	GRCh38
NC_000019.9:g.36224674G= , CM000681.1:g.36224674G=	GRCh37
NC_000019.8:g.40916514G=	NCBI36
NG_052906.1:g.20755G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.1530G=
ENST00000673918.2:c.6994G=	ENSP00000501283.1:p.Glu2332=
ENST00000674114.2:c.4601G=	ENSP00000501039.2:n.4601G=
ENST00000684977.1:c.2255G=	ENSP00000509384.1:n.2255G=
ENST00000689544.1:n.2301G=
ENST00000689929.1:c.11G=
ENST00000691421.1:c.2191G=	ENSP00000508674.1:p.Glu731=
ENST00000691855.1:c.6602G=
ENST00000692961.1:c.6984G=	ENSP00000509289.1:p.Arg2328=
ENST00000693175.1:c.11G=
ENST00000693677.1:c.805G=	ENSP00000509779.1:p.Glu269=
ENST00000420124.4:c.7060G= MANE Select	ENSP00000398837.2:p.Glu2354=
ENST00000673918.1:c.6994G=	ENSP00000501283.1:p.Glu2332=
ENST00000674114.1:c.4382G=
ENST00000420124.2:c.7060G=	ENSP00000398837.1:p.Glu2354=
ENST00000592092.1:n.440G=
NM_014727.2:c.7060G=	NP_055542.1:p.Glu2354=
XM_011527561.1:c.6994G=	XP_011525863.1:p.Glu2332=
XM_011527562.1:c.7060G=	XP_011525864.1:p.Glu2354=
XM_011527563.1:c.6784G=	XP_011525865.1:p.Glu2262=
XM_011527561.2:c.6496G=	XP_011525863.2:p.Glu2166=
XM_011527562.2:c.7060G=	XP_011525864.1:p.Glu2354=
XM_017027544.1:c.6970G=	XP_016883033.1:p.Glu2324=
XM_017027545.1:c.6496G=	XP_016883034.1:p.Glu2166=
XM_017027546.1:c.4024G=	XP_016883035.1:p.Glu1342=
NM_014727.3:c.7060G= MANE Select	NP_055542.1:p.Glu2354=