Canonical Allele Identifier: CA2333794553

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732892G= , CM000681.2:g.35732892G=	GRCh38
NC_000019.9:g.36223793G= , CM000681.1:g.36223793G=	GRCh37
NC_000019.8:g.40915633G=	NCBI36
NG_052906.1:g.19874G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.649G=
ENST00000673918.2:c.6277G=	ENSP00000501283.1:p.Asp2093=
ENST00000674114.2:c.3884G=	ENSP00000501039.2:n.3884G=
ENST00000684977.1:c.1561G=	ENSP00000509384.1:p.Asp521=
ENST00000689544.1:n.1496G=
ENST00000691421.1:c.1564G=	ENSP00000508674.1:p.Asp522=
ENST00000691855.1:c.5885G=
ENST00000692961.1:c.6343G=	ENSP00000509289.1:p.Asp2115=
ENST00000693677.1:c.704+563G=	ENSP00000509779.1:n.704+563G=
ENST00000420124.4:c.6343G= MANE Select	ENSP00000398837.2:p.Asp2115=
ENST00000673918.1:c.6277G=	ENSP00000501283.1:p.Asp2093=
ENST00000674114.1:c.3665G=
ENST00000420124.2:c.6343G=	ENSP00000398837.1:p.Asp2115=
NM_014727.2:c.6343G=	NP_055542.1:p.Asp2115=
XM_011527561.1:c.6277G=	XP_011525863.1:p.Asp2093=
XM_011527562.1:c.6343G=	XP_011525864.1:p.Asp2115=
XM_011527563.1:c.6067G=	XP_011525865.1:p.Asp2023=
XM_011527561.2:c.5779G=	XP_011525863.2:p.Asp1927=
XM_011527562.2:c.6343G=	XP_011525864.1:p.Asp2115=
XM_017027544.1:c.6343G=	XP_016883033.1:p.Asp2115=
XM_017027545.1:c.5779G=	XP_016883034.1:p.Asp1927=
XM_017027546.1:c.3307G=	XP_016883035.1:p.Asp1103=
NM_014727.3:c.6343G= MANE Select	NP_055542.1:p.Asp2115=