Canonical Allele Identifier: CA2333794365

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732548C= , CM000681.2:g.35732548C=	GRCh38
NC_000019.9:g.36223449C= , CM000681.1:g.36223449C=	GRCh37
NC_000019.8:g.40915289C=	NCBI36
NG_052906.1:g.19530C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.305C=
ENST00000673918.2:c.5933C=	ENSP00000501283.1:p.Thr1978=
ENST00000674114.2:c.3540C=	ENSP00000501039.2:n.3540C=
ENST00000684977.1:c.1217C=	ENSP00000509384.1:p.Thr406=
ENST00000689544.1:n.1152C=
ENST00000691421.1:c.1220C=	ENSP00000508674.1:p.Thr407=
ENST00000691855.1:c.5541C=
ENST00000692961.1:c.5999C=	ENSP00000509289.1:p.Thr2000=
ENST00000693677.1:c.704+219C=	ENSP00000509779.1:n.704+219C=
ENST00000420124.4:c.5999C= MANE Select	ENSP00000398837.2:p.Thr2000=
ENST00000673918.1:c.5933C=	ENSP00000501283.1:p.Thr1978=
ENST00000674114.1:c.3321C=
ENST00000420124.2:c.5999C=	ENSP00000398837.1:p.Thr2000=
NM_014727.2:c.5999C=	NP_055542.1:p.Thr2000=
XM_011527561.1:c.5933C=	XP_011525863.1:p.Thr1978=
XM_011527562.1:c.5999C=	XP_011525864.1:p.Thr2000=
XM_011527563.1:c.5723C=	XP_011525865.1:p.Thr1908=
XM_011527561.2:c.5435C=	XP_011525863.2:p.Thr1812=
XM_011527562.2:c.5999C=	XP_011525864.1:p.Thr2000=
XM_017027544.1:c.5999C=	XP_016883033.1:p.Thr2000=
XM_017027545.1:c.5435C=	XP_016883034.1:p.Thr1812=
XM_017027546.1:c.2963C=	XP_016883035.1:p.Thr988=
NM_014727.3:c.5999C= MANE Select	NP_055542.1:p.Thr2000=