Canonical Allele Identifier: CA2333793072

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729968G= , CM000681.2:g.35729968G=	GRCh38
NC_000019.9:g.36220869G= , CM000681.1:g.36220869G=	GRCh37
NC_000019.8:g.40912709G=	NCBI36
NG_052906.1:g.16950G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4853G=	ENSP00000501283.1:p.Arg1618=
ENST00000674114.2:c.2460G=	ENSP00000501039.2:n.2460G=
ENST00000684977.1:c.137G=	ENSP00000509384.1:p.Arg46=
ENST00000685168.1:c.345G=
ENST00000689544.1:n.72G=
ENST00000691421.1:c.140G=	ENSP00000508674.1:p.Arg47=
ENST00000691855.1:c.4461G=
ENST00000692961.1:c.4919G=	ENSP00000509289.1:p.Arg1640=
ENST00000420124.4:c.4919G= MANE Select	ENSP00000398837.2:p.Arg1640=
ENST00000673918.1:c.4853G=	ENSP00000501283.1:p.Arg1618=
ENST00000674114.1:c.2241G=
ENST00000420124.2:c.4919G=	ENSP00000398837.1:p.Arg1640=
NM_014727.2:c.4919G=	NP_055542.1:p.Arg1640=
XM_011527561.1:c.4853G=	XP_011525863.1:p.Arg1618=
XM_011527562.1:c.4919G=	XP_011525864.1:p.Arg1640=
XM_011527563.1:c.4643G=	XP_011525865.1:p.Arg1548=
XM_011527561.2:c.4355G=	XP_011525863.2:p.Arg1452=
XM_011527562.2:c.4919G=	XP_011525864.1:p.Arg1640=
XM_017027544.1:c.4919G=	XP_016883033.1:p.Arg1640=
XM_017027545.1:c.4355G=	XP_016883034.1:p.Arg1452=
XM_017027546.1:c.1883G=	XP_016883035.1:p.Arg628=
NM_014727.3:c.4919G= MANE Select	NP_055542.1:p.Arg1640=