Canonical Allele Identifier: CA2333794356

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732525C= , CM000681.2:g.35732525C=	GRCh38
NC_000019.9:g.36223426C= , CM000681.1:g.36223426C=	GRCh37
NC_000019.8:g.40915266C=	NCBI36
NG_052906.1:g.19507C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.282C=
ENST00000673918.2:c.5910C=	ENSP00000501283.1:p.Asp1970=
ENST00000674114.2:c.3517C=	ENSP00000501039.2:n.3517C=
ENST00000684977.1:c.1194C=	ENSP00000509384.1:p.Asp398=
ENST00000689544.1:n.1129C=
ENST00000691421.1:c.1197C=	ENSP00000508674.1:p.Asp399=
ENST00000691855.1:c.5518C=
ENST00000692961.1:c.5976C=	ENSP00000509289.1:p.Asp1992=
ENST00000693677.1:c.704+196C=	ENSP00000509779.1:n.704+196C=
ENST00000420124.4:c.5976C= MANE Select	ENSP00000398837.2:p.Asp1992=
ENST00000673918.1:c.5910C=	ENSP00000501283.1:p.Asp1970=
ENST00000674114.1:c.3298C=
ENST00000420124.2:c.5976C=	ENSP00000398837.1:p.Asp1992=
NM_014727.2:c.5976C=	NP_055542.1:p.Asp1992=
XM_011527561.1:c.5910C=	XP_011525863.1:p.Asp1970=
XM_011527562.1:c.5976C=	XP_011525864.1:p.Asp1992=
XM_011527563.1:c.5700C=	XP_011525865.1:p.Asp1900=
XM_011527561.2:c.5412C=	XP_011525863.2:p.Asp1804=
XM_011527562.2:c.5976C=	XP_011525864.1:p.Asp1992=
XM_017027544.1:c.5976C=	XP_016883033.1:p.Asp1992=
XM_017027545.1:c.5412C=	XP_016883034.1:p.Asp1804=
XM_017027546.1:c.2940C=	XP_016883035.1:p.Asp980=
NM_014727.3:c.5976C= MANE Select	NP_055542.1:p.Asp1992=