Canonical Allele Identifier: CA2333794665

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733108G= , CM000681.2:g.35733108G=	GRCh38
NC_000019.9:g.36224009G= , CM000681.1:g.36224009G=	GRCh37
NC_000019.8:g.40915849G=	NCBI36
NG_052906.1:g.20090G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.865G=
ENST00000673918.2:c.6493G=	ENSP00000501283.1:p.Ala2165=
ENST00000674114.2:c.4100G=	ENSP00000501039.2:n.4100G=
ENST00000684977.1:c.1777G=	ENSP00000509384.1:p.Ala593=
ENST00000689544.1:n.1712G=
ENST00000691421.1:c.1780G=	ENSP00000508674.1:p.Ala594=
ENST00000691855.1:c.6101G=
ENST00000692961.1:c.6559G=	ENSP00000509289.1:p.Ala2187=
ENST00000693677.1:c.705-489G=	ENSP00000509779.1:n.705-489G=
ENST00000420124.4:c.6559G= MANE Select	ENSP00000398837.2:p.Ala2187=
ENST00000673918.1:c.6493G=	ENSP00000501283.1:p.Ala2165=
ENST00000674114.1:c.3881G=
ENST00000420124.2:c.6559G=	ENSP00000398837.1:p.Ala2187=
NM_014727.2:c.6559G=	NP_055542.1:p.Ala2187=
XM_011527561.1:c.6493G=	XP_011525863.1:p.Ala2165=
XM_011527562.1:c.6559G=	XP_011525864.1:p.Ala2187=
XM_011527563.1:c.6283G=	XP_011525865.1:p.Ala2095=
XM_011527561.2:c.5995G=	XP_011525863.2:p.Ala1999=
XM_011527562.2:c.6559G=	XP_011525864.1:p.Ala2187=
XM_017027544.1:c.6559G=	XP_016883033.1:p.Ala2187=
XM_017027545.1:c.5995G=	XP_016883034.1:p.Ala1999=
XM_017027546.1:c.3523G=	XP_016883035.1:p.Ala1175=
NM_014727.3:c.6559G= MANE Select	NP_055542.1:p.Ala2187=