Canonical Allele Identifier: CA2333794480

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732735C= , CM000681.2:g.35732735C=	GRCh38
NC_000019.9:g.36223636C= , CM000681.1:g.36223636C=	GRCh37
NC_000019.8:g.40915476C=	NCBI36
NG_052906.1:g.19717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.492C=
ENST00000673918.2:c.6120C=	ENSP00000501283.1:p.Asp2040=
ENST00000674114.2:c.3727C=	ENSP00000501039.2:n.3727C=
ENST00000684977.1:c.1404C=	ENSP00000509384.1:p.Asp468=
ENST00000689544.1:n.1339C=
ENST00000691421.1:c.1407C=	ENSP00000508674.1:p.Asp469=
ENST00000691855.1:c.5728C=
ENST00000692961.1:c.6186C=	ENSP00000509289.1:p.Asp2062=
ENST00000693677.1:c.704+406C=	ENSP00000509779.1:n.704+406C=
ENST00000420124.4:c.6186C= MANE Select	ENSP00000398837.2:p.Asp2062=
ENST00000673918.1:c.6120C=	ENSP00000501283.1:p.Asp2040=
ENST00000674114.1:c.3508C=
ENST00000420124.2:c.6186C=	ENSP00000398837.1:p.Asp2062=
NM_014727.2:c.6186C=	NP_055542.1:p.Asp2062=
XM_011527561.1:c.6120C=	XP_011525863.1:p.Asp2040=
XM_011527562.1:c.6186C=	XP_011525864.1:p.Asp2062=
XM_011527563.1:c.5910C=	XP_011525865.1:p.Asp1970=
XM_011527561.2:c.5622C=	XP_011525863.2:p.Asp1874=
XM_011527562.2:c.6186C=	XP_011525864.1:p.Asp2062=
XM_017027544.1:c.6186C=	XP_016883033.1:p.Asp2062=
XM_017027545.1:c.5622C=	XP_016883034.1:p.Asp1874=
XM_017027546.1:c.3150C=	XP_016883035.1:p.Asp1050=
NM_014727.3:c.6186C= MANE Select	NP_055542.1:p.Asp2062=