Canonical Allele Identifier: CA2333794530

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732845C= , CM000681.2:g.35732845C=	GRCh38
NC_000019.9:g.36223746C= , CM000681.1:g.36223746C=	GRCh37
NC_000019.8:g.40915586C=	NCBI36
NG_052906.1:g.19827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.602C=
ENST00000673918.2:c.6230C=	ENSP00000501283.1:p.Ala2077=
ENST00000674114.2:c.3837C=	ENSP00000501039.2:n.3837C=
ENST00000684977.1:c.1514C=	ENSP00000509384.1:p.Ala505=
ENST00000689544.1:n.1449C=
ENST00000691421.1:c.1517C=	ENSP00000508674.1:p.Ala506=
ENST00000691855.1:c.5838C=
ENST00000692961.1:c.6296C=	ENSP00000509289.1:p.Ala2099=
ENST00000693677.1:c.704+516C=	ENSP00000509779.1:n.704+516C=
ENST00000420124.4:c.6296C= MANE Select	ENSP00000398837.2:p.Ala2099=
ENST00000673918.1:c.6230C=	ENSP00000501283.1:p.Ala2077=
ENST00000674114.1:c.3618C=
ENST00000420124.2:c.6296C=	ENSP00000398837.1:p.Ala2099=
NM_014727.2:c.6296C=	NP_055542.1:p.Ala2099=
XM_011527561.1:c.6230C=	XP_011525863.1:p.Ala2077=
XM_011527562.1:c.6296C=	XP_011525864.1:p.Ala2099=
XM_011527563.1:c.6020C=	XP_011525865.1:p.Ala2007=
XM_011527561.2:c.5732C=	XP_011525863.2:p.Ala1911=
XM_011527562.2:c.6296C=	XP_011525864.1:p.Ala2099=
XM_017027544.1:c.6296C=	XP_016883033.1:p.Ala2099=
XM_017027545.1:c.5732C=	XP_016883034.1:p.Ala1911=
XM_017027546.1:c.3260C=	XP_016883035.1:p.Ala1087=
NM_014727.3:c.6296C= MANE Select	NP_055542.1:p.Ala2099=