Canonical Allele Identifier: CA2333794522

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732828A= , CM000681.2:g.35732828A=	GRCh38
NC_000019.9:g.36223729A= , CM000681.1:g.36223729A=	GRCh37
NC_000019.8:g.40915569A=	NCBI36
NG_052906.1:g.19810A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.585A=
ENST00000673918.2:c.6213A=	ENSP00000501283.1:p.Ala2071=
ENST00000674114.2:c.3820A=	ENSP00000501039.2:n.3820A=
ENST00000684977.1:c.1497A=	ENSP00000509384.1:p.Ala499=
ENST00000689544.1:n.1432A=
ENST00000691421.1:c.1500A=	ENSP00000508674.1:p.Ala500=
ENST00000691855.1:c.5821A=
ENST00000692961.1:c.6279A=	ENSP00000509289.1:p.Ala2093=
ENST00000693677.1:c.704+499A=	ENSP00000509779.1:n.704+499A=
ENST00000420124.4:c.6279A= MANE Select	ENSP00000398837.2:p.Ala2093=
ENST00000673918.1:c.6213A=	ENSP00000501283.1:p.Ala2071=
ENST00000674114.1:c.3601A=
ENST00000420124.2:c.6279A=	ENSP00000398837.1:p.Ala2093=
NM_014727.2:c.6279A=	NP_055542.1:p.Ala2093=
XM_011527561.1:c.6213A=	XP_011525863.1:p.Ala2071=
XM_011527562.1:c.6279A=	XP_011525864.1:p.Ala2093=
XM_011527563.1:c.6003A=	XP_011525865.1:p.Ala2001=
XM_011527561.2:c.5715A=	XP_011525863.2:p.Ala1905=
XM_011527562.2:c.6279A=	XP_011525864.1:p.Ala2093=
XM_017027544.1:c.6279A=	XP_016883033.1:p.Ala2093=
XM_017027545.1:c.5715A=	XP_016883034.1:p.Ala1905=
XM_017027546.1:c.3243A=	XP_016883035.1:p.Ala1081=
NM_014727.3:c.6279A= MANE Select	NP_055542.1:p.Ala2093=