Canonical Allele Identifier: CA2333794693

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733178C= , CM000681.2:g.35733178C=	GRCh38
NC_000019.9:g.36224079C= , CM000681.1:g.36224079C=	GRCh37
NC_000019.8:g.40915919C=	NCBI36
NG_052906.1:g.20160C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.935C=
ENST00000673918.2:c.6563C=	ENSP00000501283.1:p.Pro2188=
ENST00000674114.2:c.4170C=	ENSP00000501039.2:n.4170C=
ENST00000684977.1:c.1847C=	ENSP00000509384.1:p.Pro616=
ENST00000689544.1:n.1782C=
ENST00000691421.1:c.1850C=	ENSP00000508674.1:p.Pro617=
ENST00000691855.1:c.6171C=
ENST00000692961.1:c.6629C=	ENSP00000509289.1:p.Pro2210=
ENST00000693677.1:c.705-419C=	ENSP00000509779.1:n.705-419C=
ENST00000420124.4:c.6629C= MANE Select	ENSP00000398837.2:p.Pro2210=
ENST00000673918.1:c.6563C=	ENSP00000501283.1:p.Pro2188=
ENST00000674114.1:c.3951C=
ENST00000420124.2:c.6629C=	ENSP00000398837.1:p.Pro2210=
NM_014727.2:c.6629C=	NP_055542.1:p.Pro2210=
XM_011527561.1:c.6563C=	XP_011525863.1:p.Pro2188=
XM_011527562.1:c.6629C=	XP_011525864.1:p.Pro2210=
XM_011527563.1:c.6353C=	XP_011525865.1:p.Pro2118=
XM_011527561.2:c.6065C=	XP_011525863.2:p.Pro2022=
XM_011527562.2:c.6629C=	XP_011525864.1:p.Pro2210=
XM_017027544.1:c.6629C=	XP_016883033.1:p.Pro2210=
XM_017027545.1:c.6065C=	XP_016883034.1:p.Pro2022=
XM_017027546.1:c.3593C=	XP_016883035.1:p.Pro1198=
NM_014727.3:c.6629C= MANE Select	NP_055542.1:p.Pro2210=