Canonical Allele Identifier: CA2333794515

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732811C= , CM000681.2:g.35732811C=	GRCh38
NC_000019.9:g.36223712C= , CM000681.1:g.36223712C=	GRCh37
NC_000019.8:g.40915552C=	NCBI36
NG_052906.1:g.19793C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.568C=
ENST00000673918.2:c.6196C=	ENSP00000501283.1:p.Pro2066=
ENST00000674114.2:c.3803C=	ENSP00000501039.2:n.3803C=
ENST00000684977.1:c.1480C=	ENSP00000509384.1:p.Pro494=
ENST00000689544.1:n.1415C=
ENST00000691421.1:c.1483C=	ENSP00000508674.1:p.Pro495=
ENST00000691855.1:c.5804C=
ENST00000692961.1:c.6262C=	ENSP00000509289.1:p.Pro2088=
ENST00000693677.1:c.704+482C=	ENSP00000509779.1:n.704+482C=
ENST00000420124.4:c.6262C= MANE Select	ENSP00000398837.2:p.Pro2088=
ENST00000673918.1:c.6196C=	ENSP00000501283.1:p.Pro2066=
ENST00000674114.1:c.3584C=
ENST00000420124.2:c.6262C=	ENSP00000398837.1:p.Pro2088=
NM_014727.2:c.6262C=	NP_055542.1:p.Pro2088=
XM_011527561.1:c.6196C=	XP_011525863.1:p.Pro2066=
XM_011527562.1:c.6262C=	XP_011525864.1:p.Pro2088=
XM_011527563.1:c.5986C=	XP_011525865.1:p.Pro1996=
XM_011527561.2:c.5698C=	XP_011525863.2:p.Pro1900=
XM_011527562.2:c.6262C=	XP_011525864.1:p.Pro2088=
XM_017027544.1:c.6262C=	XP_016883033.1:p.Pro2088=
XM_017027545.1:c.5698C=	XP_016883034.1:p.Pro1900=
XM_017027546.1:c.3226C=	XP_016883035.1:p.Pro1076=
NM_014727.3:c.6262C= MANE Select	NP_055542.1:p.Pro2088=