Canonical Allele Identifier: CA2333793104

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730065C= , CM000681.2:g.35730065C=	GRCh38
NC_000019.9:g.36220966C= , CM000681.1:g.36220966C=	GRCh37
NC_000019.8:g.40912806C=	NCBI36
NG_052906.1:g.17047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4950C=	ENSP00000501283.1:p.Cys1650=
ENST00000674114.2:c.2557C=	ENSP00000501039.2:n.2557C=
ENST00000684977.1:c.234C=	ENSP00000509384.1:p.Cys78=
ENST00000685168.1:c.442C=
ENST00000689544.1:n.169C=
ENST00000691421.1:c.237C=	ENSP00000508674.1:p.Cys79=
ENST00000691855.1:c.4558C=
ENST00000692961.1:c.5016C=	ENSP00000509289.1:p.Cys1672=
ENST00000420124.4:c.5016C= MANE Select	ENSP00000398837.2:p.Cys1672=
ENST00000673918.1:c.4950C=	ENSP00000501283.1:p.Cys1650=
ENST00000674114.1:c.2338C=
ENST00000420124.2:c.5016C=	ENSP00000398837.1:p.Cys1672=
NM_014727.2:c.5016C=	NP_055542.1:p.Cys1672=
XM_011527561.1:c.4950C=	XP_011525863.1:p.Cys1650=
XM_011527562.1:c.5016C=	XP_011525864.1:p.Cys1672=
XM_011527563.1:c.4740C=	XP_011525865.1:p.Cys1580=
XM_011527561.2:c.4452C=	XP_011525863.2:p.Cys1484=
XM_011527562.2:c.5016C=	XP_011525864.1:p.Cys1672=
XM_017027544.1:c.5016C=	XP_016883033.1:p.Cys1672=
XM_017027545.1:c.4452C=	XP_016883034.1:p.Cys1484=
XM_017027546.1:c.1980C=	XP_016883035.1:p.Cys660=
NM_014727.3:c.5016C= MANE Select	NP_055542.1:p.Cys1672=