Canonical Allele Identifier: CA2333794450

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732694C= , CM000681.2:g.35732694C=	GRCh38
NC_000019.9:g.36223595C= , CM000681.1:g.36223595C=	GRCh37
NC_000019.8:g.40915435C=	NCBI36
NG_052906.1:g.19676C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.451C=
ENST00000673918.2:c.6079C=	ENSP00000501283.1:p.Pro2027=
ENST00000674114.2:c.3686C=	ENSP00000501039.2:n.3686C=
ENST00000684977.1:c.1363C=	ENSP00000509384.1:p.Pro455=
ENST00000689544.1:n.1298C=
ENST00000691421.1:c.1366C=	ENSP00000508674.1:p.Pro456=
ENST00000691855.1:c.5687C=
ENST00000692961.1:c.6145C=	ENSP00000509289.1:p.Pro2049=
ENST00000693677.1:c.704+365C=	ENSP00000509779.1:n.704+365C=
ENST00000420124.4:c.6145C= MANE Select	ENSP00000398837.2:p.Pro2049=
ENST00000673918.1:c.6079C=	ENSP00000501283.1:p.Pro2027=
ENST00000674114.1:c.3467C=
ENST00000420124.2:c.6145C=	ENSP00000398837.1:p.Pro2049=
NM_014727.2:c.6145C=	NP_055542.1:p.Pro2049=
XM_011527561.1:c.6079C=	XP_011525863.1:p.Pro2027=
XM_011527562.1:c.6145C=	XP_011525864.1:p.Pro2049=
XM_011527563.1:c.5869C=	XP_011525865.1:p.Pro1957=
XM_011527561.2:c.5581C=	XP_011525863.2:p.Pro1861=
XM_011527562.2:c.6145C=	XP_011525864.1:p.Pro2049=
XM_017027544.1:c.6145C=	XP_016883033.1:p.Pro2049=
XM_017027545.1:c.5581C=	XP_016883034.1:p.Pro1861=
XM_017027546.1:c.3109C=	XP_016883035.1:p.Pro1037=
NM_014727.3:c.6145C= MANE Select	NP_055542.1:p.Pro2049=