Canonical Allele Identifier: CA2333794622

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733039G= , CM000681.2:g.35733039G=	GRCh38
NC_000019.9:g.36223940G= , CM000681.1:g.36223940G=	GRCh37
NC_000019.8:g.40915780G=	NCBI36
NG_052906.1:g.20021G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.796G=
ENST00000673918.2:c.6424G=	ENSP00000501283.1:p.Ala2142=
ENST00000674114.2:c.4031G=	ENSP00000501039.2:n.4031G=
ENST00000684977.1:c.1708G=	ENSP00000509384.1:p.Ala570=
ENST00000689544.1:n.1643G=
ENST00000691421.1:c.1711G=	ENSP00000508674.1:p.Ala571=
ENST00000691855.1:c.6032G=
ENST00000692961.1:c.6490G=	ENSP00000509289.1:p.Ala2164=
ENST00000693677.1:c.705-558G=	ENSP00000509779.1:n.705-558G=
ENST00000420124.4:c.6490G= MANE Select	ENSP00000398837.2:p.Ala2164=
ENST00000673918.1:c.6424G=	ENSP00000501283.1:p.Ala2142=
ENST00000674114.1:c.3812G=
ENST00000420124.2:c.6490G=	ENSP00000398837.1:p.Ala2164=
NM_014727.2:c.6490G=	NP_055542.1:p.Ala2164=
XM_011527561.1:c.6424G=	XP_011525863.1:p.Ala2142=
XM_011527562.1:c.6490G=	XP_011525864.1:p.Ala2164=
XM_011527563.1:c.6214G=	XP_011525865.1:p.Ala2072=
XM_011527561.2:c.5926G=	XP_011525863.2:p.Ala1976=
XM_011527562.2:c.6490G=	XP_011525864.1:p.Ala2164=
XM_017027544.1:c.6490G=	XP_016883033.1:p.Ala2164=
XM_017027545.1:c.5926G=	XP_016883034.1:p.Ala1976=
XM_017027546.1:c.3454G=	XP_016883035.1:p.Ala1152=
NM_014727.3:c.6490G= MANE Select	NP_055542.1:p.Ala2164=