Canonical Allele Identifier: CA2333794703

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733198C= , CM000681.2:g.35733198C=	GRCh38
NC_000019.9:g.36224099C= , CM000681.1:g.36224099C=	GRCh37
NC_000019.8:g.40915939C=	NCBI36
NG_052906.1:g.20180C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.955C=
ENST00000673918.2:c.6583C=	ENSP00000501283.1:p.Gln2195=
ENST00000674114.2:c.4190C=	ENSP00000501039.2:n.4190C=
ENST00000684977.1:c.1867C=	ENSP00000509384.1:p.Gln623=
ENST00000689544.1:n.1802C=
ENST00000691421.1:c.1870C=	ENSP00000508674.1:p.Gln624=
ENST00000691855.1:c.6191C=
ENST00000692961.1:c.6649C=	ENSP00000509289.1:p.Gln2217=
ENST00000693677.1:c.705-399C=	ENSP00000509779.1:n.705-399C=
ENST00000420124.4:c.6649C= MANE Select	ENSP00000398837.2:p.Gln2217=
ENST00000673918.1:c.6583C=	ENSP00000501283.1:p.Gln2195=
ENST00000674114.1:c.3971C=
ENST00000420124.2:c.6649C=	ENSP00000398837.1:p.Gln2217=
NM_014727.2:c.6649C=	NP_055542.1:p.Gln2217=
XM_011527561.1:c.6583C=	XP_011525863.1:p.Gln2195=
XM_011527562.1:c.6649C=	XP_011525864.1:p.Gln2217=
XM_011527563.1:c.6373C=	XP_011525865.1:p.Gln2125=
XM_011527561.2:c.6085C=	XP_011525863.2:p.Gln2029=
XM_011527562.2:c.6649C=	XP_011525864.1:p.Gln2217=
XM_017027544.1:c.6649C=	XP_016883033.1:p.Gln2217=
XM_017027545.1:c.6085C=	XP_016883034.1:p.Gln2029=
XM_017027546.1:c.3613C=	XP_016883035.1:p.Gln1205=
NM_014727.3:c.6649C= MANE Select	NP_055542.1:p.Gln2217=