Canonical Allele Identifier: CA2333794660

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733103A= , CM000681.2:g.35733103A=	GRCh38
NC_000019.9:g.36224004A= , CM000681.1:g.36224004A=	GRCh37
NC_000019.8:g.40915844A=	NCBI36
NG_052906.1:g.20085A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.860A=
ENST00000673918.2:c.6488A=	ENSP00000501283.1:p.Lys2163=
ENST00000674114.2:c.4095A=	ENSP00000501039.2:n.4095A=
ENST00000684977.1:c.1772A=	ENSP00000509384.1:p.Lys591=
ENST00000689544.1:n.1707A=
ENST00000691421.1:c.1775A=	ENSP00000508674.1:p.Lys592=
ENST00000691855.1:c.6096A=
ENST00000692961.1:c.6554A=	ENSP00000509289.1:p.Lys2185=
ENST00000693677.1:c.705-494A=	ENSP00000509779.1:n.705-494A=
ENST00000420124.4:c.6554A= MANE Select	ENSP00000398837.2:p.Lys2185=
ENST00000673918.1:c.6488A=	ENSP00000501283.1:p.Lys2163=
ENST00000674114.1:c.3876A=
ENST00000420124.2:c.6554A=	ENSP00000398837.1:p.Lys2185=
NM_014727.2:c.6554A=	NP_055542.1:p.Lys2185=
XM_011527561.1:c.6488A=	XP_011525863.1:p.Lys2163=
XM_011527562.1:c.6554A=	XP_011525864.1:p.Lys2185=
XM_011527563.1:c.6278A=	XP_011525865.1:p.Lys2093=
XM_011527561.2:c.5990A=	XP_011525863.2:p.Lys1997=
XM_011527562.2:c.6554A=	XP_011525864.1:p.Lys2185=
XM_017027544.1:c.6554A=	XP_016883033.1:p.Lys2185=
XM_017027545.1:c.5990A=	XP_016883034.1:p.Lys1997=
XM_017027546.1:c.3518A=	XP_016883035.1:p.Lys1173=
NM_014727.3:c.6554A= MANE Select	NP_055542.1:p.Lys2185=