Canonical Allele Identifier: CA2333794631

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733056C= , CM000681.2:g.35733056C=	GRCh38
NC_000019.9:g.36223957C= , CM000681.1:g.36223957C=	GRCh37
NC_000019.8:g.40915797C=	NCBI36
NG_052906.1:g.20038C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.813C=
ENST00000673918.2:c.6441C=	ENSP00000501283.1:p.Ala2147=
ENST00000674114.2:c.4048C=	ENSP00000501039.2:n.4048C=
ENST00000684977.1:c.1725C=	ENSP00000509384.1:p.Ala575=
ENST00000689544.1:n.1660C=
ENST00000691421.1:c.1728C=	ENSP00000508674.1:p.Ala576=
ENST00000691855.1:c.6049C=
ENST00000692961.1:c.6507C=	ENSP00000509289.1:p.Ala2169=
ENST00000693677.1:c.705-541C=	ENSP00000509779.1:n.705-541C=
ENST00000420124.4:c.6507C= MANE Select	ENSP00000398837.2:p.Ala2169=
ENST00000673918.1:c.6441C=	ENSP00000501283.1:p.Ala2147=
ENST00000674114.1:c.3829C=
ENST00000420124.2:c.6507C=	ENSP00000398837.1:p.Ala2169=
NM_014727.2:c.6507C=	NP_055542.1:p.Ala2169=
XM_011527561.1:c.6441C=	XP_011525863.1:p.Ala2147=
XM_011527562.1:c.6507C=	XP_011525864.1:p.Ala2169=
XM_011527563.1:c.6231C=	XP_011525865.1:p.Ala2077=
XM_011527561.2:c.5943C=	XP_011525863.2:p.Ala1981=
XM_011527562.2:c.6507C=	XP_011525864.1:p.Ala2169=
XM_017027544.1:c.6507C=	XP_016883033.1:p.Ala2169=
XM_017027545.1:c.5943C=	XP_016883034.1:p.Ala1981=
XM_017027546.1:c.3471C=	XP_016883035.1:p.Ala1157=
NM_014727.3:c.6507C= MANE Select	NP_055542.1:p.Ala2169=