Canonical Allele Identifier: CA2333794539

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732865C= , CM000681.2:g.35732865C=	GRCh38
NC_000019.9:g.36223766C= , CM000681.1:g.36223766C=	GRCh37
NC_000019.8:g.40915606C=	NCBI36
NG_052906.1:g.19847C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.622C=
ENST00000673918.2:c.6250C=	ENSP00000501283.1:p.Pro2084=
ENST00000674114.2:c.3857C=	ENSP00000501039.2:n.3857C=
ENST00000684977.1:c.1534C=	ENSP00000509384.1:p.Pro512=
ENST00000689544.1:n.1469C=
ENST00000691421.1:c.1537C=	ENSP00000508674.1:p.Pro513=
ENST00000691855.1:c.5858C=
ENST00000692961.1:c.6316C=	ENSP00000509289.1:p.Pro2106=
ENST00000693677.1:c.704+536C=	ENSP00000509779.1:n.704+536C=
ENST00000420124.4:c.6316C= MANE Select	ENSP00000398837.2:p.Pro2106=
ENST00000673918.1:c.6250C=	ENSP00000501283.1:p.Pro2084=
ENST00000674114.1:c.3638C=
ENST00000420124.2:c.6316C=	ENSP00000398837.1:p.Pro2106=
NM_014727.2:c.6316C=	NP_055542.1:p.Pro2106=
XM_011527561.1:c.6250C=	XP_011525863.1:p.Pro2084=
XM_011527562.1:c.6316C=	XP_011525864.1:p.Pro2106=
XM_011527563.1:c.6040C=	XP_011525865.1:p.Pro2014=
XM_011527561.2:c.5752C=	XP_011525863.2:p.Pro1918=
XM_011527562.2:c.6316C=	XP_011525864.1:p.Pro2106=
XM_017027544.1:c.6316C=	XP_016883033.1:p.Pro2106=
XM_017027545.1:c.5752C=	XP_016883034.1:p.Pro1918=
XM_017027546.1:c.3280C=	XP_016883035.1:p.Pro1094=
NM_014727.3:c.6316C= MANE Select	NP_055542.1:p.Pro2106=