Canonical Allele Identifier: CA2333794584

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732964G= , CM000681.2:g.35732964G=	GRCh38
NC_000019.9:g.36223865G= , CM000681.1:g.36223865G=	GRCh37
NC_000019.8:g.40915705G=	NCBI36
NG_052906.1:g.19946G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.721G=
ENST00000673918.2:c.6349G=	ENSP00000501283.1:p.Ala2117=
ENST00000674114.2:c.3956G=	ENSP00000501039.2:n.3956G=
ENST00000684977.1:c.1633G=	ENSP00000509384.1:p.Ala545=
ENST00000689544.1:n.1568G=
ENST00000691421.1:c.1636G=	ENSP00000508674.1:p.Ala546=
ENST00000691855.1:c.5957G=
ENST00000692961.1:c.6415G=	ENSP00000509289.1:p.Ala2139=
ENST00000693677.1:c.705-633G=	ENSP00000509779.1:n.705-633G=
ENST00000420124.4:c.6415G= MANE Select	ENSP00000398837.2:p.Ala2139=
ENST00000673918.1:c.6349G=	ENSP00000501283.1:p.Ala2117=
ENST00000674114.1:c.3737G=
ENST00000420124.2:c.6415G=	ENSP00000398837.1:p.Ala2139=
NM_014727.2:c.6415G=	NP_055542.1:p.Ala2139=
XM_011527561.1:c.6349G=	XP_011525863.1:p.Ala2117=
XM_011527562.1:c.6415G=	XP_011525864.1:p.Ala2139=
XM_011527563.1:c.6139G=	XP_011525865.1:p.Ala2047=
XM_011527561.2:c.5851G=	XP_011525863.2:p.Ala1951=
XM_011527562.2:c.6415G=	XP_011525864.1:p.Ala2139=
XM_017027544.1:c.6415G=	XP_016883033.1:p.Ala2139=
XM_017027545.1:c.5851G=	XP_016883034.1:p.Ala1951=
XM_017027546.1:c.3379G=	XP_016883035.1:p.Ala1127=
NM_014727.3:c.6415G= MANE Select	NP_055542.1:p.Ala2139=