Canonical Allele Identifier: CA2333793076

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729980G= , CM000681.2:g.35729980G=	GRCh38
NC_000019.9:g.36220881G= , CM000681.1:g.36220881G=	GRCh37
NC_000019.8:g.40912721G=	NCBI36
NG_052906.1:g.16962G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4865G=	ENSP00000501283.1:p.Cys1622=
ENST00000674114.2:c.2472G=	ENSP00000501039.2:n.2472G=
ENST00000684977.1:c.149G=	ENSP00000509384.1:p.Cys50=
ENST00000685168.1:c.357G=
ENST00000689544.1:n.84G=
ENST00000691421.1:c.152G=	ENSP00000508674.1:p.Cys51=
ENST00000691855.1:c.4473G=
ENST00000692961.1:c.4931G=	ENSP00000509289.1:p.Cys1644=
ENST00000420124.4:c.4931G= MANE Select	ENSP00000398837.2:p.Cys1644=
ENST00000673918.1:c.4865G=	ENSP00000501283.1:p.Cys1622=
ENST00000674114.1:c.2253G=
ENST00000420124.2:c.4931G=	ENSP00000398837.1:p.Cys1644=
NM_014727.2:c.4931G=	NP_055542.1:p.Cys1644=
XM_011527561.1:c.4865G=	XP_011525863.1:p.Cys1622=
XM_011527562.1:c.4931G=	XP_011525864.1:p.Cys1644=
XM_011527563.1:c.4655G=	XP_011525865.1:p.Cys1552=
XM_011527561.2:c.4367G=	XP_011525863.2:p.Cys1456=
XM_011527562.2:c.4931G=	XP_011525864.1:p.Cys1644=
XM_017027544.1:c.4931G=	XP_016883033.1:p.Cys1644=
XM_017027545.1:c.4367G=	XP_016883034.1:p.Cys1456=
XM_017027546.1:c.1895G=	XP_016883035.1:p.Cys632=
NM_014727.3:c.4931G= MANE Select	NP_055542.1:p.Cys1644=