Canonical Allele Identifier: CA2333794355

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732523G= , CM000681.2:g.35732523G=	GRCh38
NC_000019.9:g.36223424G= , CM000681.1:g.36223424G=	GRCh37
NC_000019.8:g.40915264G=	NCBI36
NG_052906.1:g.19505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.280G=
ENST00000673918.2:c.5908G=	ENSP00000501283.1:p.Asp1970=
ENST00000674114.2:c.3515G=	ENSP00000501039.2:n.3515G=
ENST00000684977.1:c.1192G=	ENSP00000509384.1:p.Asp398=
ENST00000689544.1:n.1127G=
ENST00000691421.1:c.1195G=	ENSP00000508674.1:p.Asp399=
ENST00000691855.1:c.5516G=
ENST00000692961.1:c.5974G=	ENSP00000509289.1:p.Asp1992=
ENST00000693677.1:c.704+194G=	ENSP00000509779.1:n.704+194G=
ENST00000420124.4:c.5974G= MANE Select	ENSP00000398837.2:p.Asp1992=
ENST00000673918.1:c.5908G=	ENSP00000501283.1:p.Asp1970=
ENST00000674114.1:c.3296G=
ENST00000420124.2:c.5974G=	ENSP00000398837.1:p.Asp1992=
NM_014727.2:c.5974G=	NP_055542.1:p.Asp1992=
XM_011527561.1:c.5908G=	XP_011525863.1:p.Asp1970=
XM_011527562.1:c.5974G=	XP_011525864.1:p.Asp1992=
XM_011527563.1:c.5698G=	XP_011525865.1:p.Asp1900=
XM_011527561.2:c.5410G=	XP_011525863.2:p.Asp1804=
XM_011527562.2:c.5974G=	XP_011525864.1:p.Asp1992=
XM_017027544.1:c.5974G=	XP_016883033.1:p.Asp1992=
XM_017027545.1:c.5410G=	XP_016883034.1:p.Asp1804=
XM_017027546.1:c.2938G=	XP_016883035.1:p.Asp980=
NM_014727.3:c.5974G= MANE Select	NP_055542.1:p.Asp1992=