Canonical Allele Identifier: CA2333794410

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732632C= , CM000681.2:g.35732632C=	GRCh38
NC_000019.9:g.36223533C= , CM000681.1:g.36223533C=	GRCh37
NC_000019.8:g.40915373C=	NCBI36
NG_052906.1:g.19614C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.389C=
ENST00000673918.2:c.6017C=	ENSP00000501283.1:p.Ser2006=
ENST00000674114.2:c.3624C=	ENSP00000501039.2:n.3624C=
ENST00000684977.1:c.1301C=	ENSP00000509384.1:p.Ser434=
ENST00000689544.1:n.1236C=
ENST00000691421.1:c.1304C=	ENSP00000508674.1:p.Ser435=
ENST00000691855.1:c.5625C=
ENST00000692961.1:c.6083C=	ENSP00000509289.1:p.Ser2028=
ENST00000693677.1:c.704+303C=	ENSP00000509779.1:n.704+303C=
ENST00000420124.4:c.6083C= MANE Select	ENSP00000398837.2:p.Ser2028=
ENST00000673918.1:c.6017C=	ENSP00000501283.1:p.Ser2006=
ENST00000674114.1:c.3405C=
ENST00000420124.2:c.6083C=	ENSP00000398837.1:p.Ser2028=
NM_014727.2:c.6083C=	NP_055542.1:p.Ser2028=
XM_011527561.1:c.6017C=	XP_011525863.1:p.Ser2006=
XM_011527562.1:c.6083C=	XP_011525864.1:p.Ser2028=
XM_011527563.1:c.5807C=	XP_011525865.1:p.Ser1936=
XM_011527561.2:c.5519C=	XP_011525863.2:p.Ser1840=
XM_011527562.2:c.6083C=	XP_011525864.1:p.Ser2028=
XM_017027544.1:c.6083C=	XP_016883033.1:p.Ser2028=
XM_017027545.1:c.5519C=	XP_016883034.1:p.Ser1840=
XM_017027546.1:c.3047C=	XP_016883035.1:p.Ser1016=
NM_014727.3:c.6083C= MANE Select	NP_055542.1:p.Ser2028=