Canonical Allele Identifier: CA2333794714

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733218C= , CM000681.2:g.35733218C=	GRCh38
NC_000019.9:g.36224119C= , CM000681.1:g.36224119C=	GRCh37
NC_000019.8:g.40915959C=	NCBI36
NG_052906.1:g.20200C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.975C=
ENST00000673918.2:c.6603C=	ENSP00000501283.1:p.Thr2201=
ENST00000674114.2:c.4210C=	ENSP00000501039.2:n.4210C=
ENST00000684977.1:c.1887C=	ENSP00000509384.1:p.Thr629=
ENST00000689544.1:n.1822C=
ENST00000691421.1:c.1890C=	ENSP00000508674.1:p.Thr630=
ENST00000691855.1:c.6211C=
ENST00000692961.1:c.6669C=	ENSP00000509289.1:p.Thr2223=
ENST00000693677.1:c.705-379C=	ENSP00000509779.1:n.705-379C=
ENST00000420124.4:c.6669C= MANE Select	ENSP00000398837.2:p.Thr2223=
ENST00000673918.1:c.6603C=	ENSP00000501283.1:p.Thr2201=
ENST00000674114.1:c.3991C=
ENST00000420124.2:c.6669C=	ENSP00000398837.1:p.Thr2223=
NM_014727.2:c.6669C=	NP_055542.1:p.Thr2223=
XM_011527561.1:c.6603C=	XP_011525863.1:p.Thr2201=
XM_011527562.1:c.6669C=	XP_011525864.1:p.Thr2223=
XM_011527563.1:c.6393C=	XP_011525865.1:p.Thr2131=
XM_011527561.2:c.6105C=	XP_011525863.2:p.Thr2035=
XM_011527562.2:c.6669C=	XP_011525864.1:p.Thr2223=
XM_017027544.1:c.6669C=	XP_016883033.1:p.Thr2223=
XM_017027545.1:c.6105C=	XP_016883034.1:p.Thr2035=
XM_017027546.1:c.3633C=	XP_016883035.1:p.Thr1211=
NM_014727.3:c.6669C= MANE Select	NP_055542.1:p.Thr2223=