Canonical Allele Identifier: CA2333794331

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732454C= , CM000681.2:g.35732454C=	GRCh38
NC_000019.9:g.36223355C= , CM000681.1:g.36223355C=	GRCh37
NC_000019.8:g.40915195C=	NCBI36
NG_052906.1:g.19436C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.211C=
ENST00000673918.2:c.5839C=	ENSP00000501283.1:p.Pro1947=
ENST00000674114.2:c.3446C=	ENSP00000501039.2:n.3446C=
ENST00000684977.1:c.1123C=	ENSP00000509384.1:p.Pro375=
ENST00000689544.1:n.1058C=
ENST00000691421.1:c.1126C=	ENSP00000508674.1:p.Pro376=
ENST00000691855.1:c.5447C=
ENST00000692961.1:c.5905C=	ENSP00000509289.1:p.Pro1969=
ENST00000693677.1:c.704+125C=	ENSP00000509779.1:n.704+125C=
ENST00000420124.4:c.5905C= MANE Select	ENSP00000398837.2:p.Pro1969=
ENST00000673918.1:c.5839C=	ENSP00000501283.1:p.Pro1947=
ENST00000674114.1:c.3227C=
ENST00000420124.2:c.5905C=	ENSP00000398837.1:p.Pro1969=
NM_014727.2:c.5905C=	NP_055542.1:p.Pro1969=
XM_011527561.1:c.5839C=	XP_011525863.1:p.Pro1947=
XM_011527562.1:c.5905C=	XP_011525864.1:p.Pro1969=
XM_011527563.1:c.5629C=	XP_011525865.1:p.Pro1877=
XM_011527561.2:c.5341C=	XP_011525863.2:p.Pro1781=
XM_011527562.2:c.5905C=	XP_011525864.1:p.Pro1969=
XM_017027544.1:c.5905C=	XP_016883033.1:p.Pro1969=
XM_017027545.1:c.5341C=	XP_016883034.1:p.Pro1781=
XM_017027546.1:c.2869C=	XP_016883035.1:p.Pro957=
NM_014727.3:c.5905C= MANE Select	NP_055542.1:p.Pro1969=