Canonical Allele Identifier: CA2333794397

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732608C= , CM000681.2:g.35732608C=	GRCh38
NC_000019.9:g.36223509C= , CM000681.1:g.36223509C=	GRCh37
NC_000019.8:g.40915349C=	NCBI36
NG_052906.1:g.19590C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.365C=
ENST00000673918.2:c.5993C=	ENSP00000501283.1:p.Pro1998=
ENST00000674114.2:c.3600C=	ENSP00000501039.2:n.3600C=
ENST00000684977.1:c.1277C=	ENSP00000509384.1:p.Pro426=
ENST00000689544.1:n.1212C=
ENST00000691421.1:c.1280C=	ENSP00000508674.1:p.Pro427=
ENST00000691855.1:c.5601C=
ENST00000692961.1:c.6059C=	ENSP00000509289.1:p.Pro2020=
ENST00000693677.1:c.704+279C=	ENSP00000509779.1:n.704+279C=
ENST00000420124.4:c.6059C= MANE Select	ENSP00000398837.2:p.Pro2020=
ENST00000673918.1:c.5993C=	ENSP00000501283.1:p.Pro1998=
ENST00000674114.1:c.3381C=
ENST00000420124.2:c.6059C=	ENSP00000398837.1:p.Pro2020=
NM_014727.2:c.6059C=	NP_055542.1:p.Pro2020=
XM_011527561.1:c.5993C=	XP_011525863.1:p.Pro1998=
XM_011527562.1:c.6059C=	XP_011525864.1:p.Pro2020=
XM_011527563.1:c.5783C=	XP_011525865.1:p.Pro1928=
XM_011527561.2:c.5495C=	XP_011525863.2:p.Pro1832=
XM_011527562.2:c.6059C=	XP_011525864.1:p.Pro2020=
XM_017027544.1:c.6059C=	XP_016883033.1:p.Pro2020=
XM_017027545.1:c.5495C=	XP_016883034.1:p.Pro1832=
XM_017027546.1:c.3023C=	XP_016883035.1:p.Pro1008=
NM_014727.3:c.6059C= MANE Select	NP_055542.1:p.Pro2020=