Canonical Allele Identifier: CA2333794601

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732998A= , CM000681.2:g.35732998A=	GRCh38
NC_000019.9:g.36223899A= , CM000681.1:g.36223899A=	GRCh37
NC_000019.8:g.40915739A=	NCBI36
NG_052906.1:g.19980A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.755A=
ENST00000673918.2:c.6383A=	ENSP00000501283.1:p.Gln2128=
ENST00000674114.2:c.3990A=	ENSP00000501039.2:n.3990A=
ENST00000684977.1:c.1667A=	ENSP00000509384.1:p.Gln556=
ENST00000689544.1:n.1602A=
ENST00000691421.1:c.1670A=	ENSP00000508674.1:p.Gln557=
ENST00000691855.1:c.5991A=
ENST00000692961.1:c.6449A=	ENSP00000509289.1:p.Gln2150=
ENST00000693677.1:c.705-599A=	ENSP00000509779.1:n.705-599A=
ENST00000420124.4:c.6449A= MANE Select	ENSP00000398837.2:p.Gln2150=
ENST00000673918.1:c.6383A=	ENSP00000501283.1:p.Gln2128=
ENST00000674114.1:c.3771A=
ENST00000420124.2:c.6449A=	ENSP00000398837.1:p.Gln2150=
NM_014727.2:c.6449A=	NP_055542.1:p.Gln2150=
XM_011527561.1:c.6383A=	XP_011525863.1:p.Gln2128=
XM_011527562.1:c.6449A=	XP_011525864.1:p.Gln2150=
XM_011527563.1:c.6173A=	XP_011525865.1:p.Gln2058=
XM_011527561.2:c.5885A=	XP_011525863.2:p.Gln1962=
XM_011527562.2:c.6449A=	XP_011525864.1:p.Gln2150=
XM_017027544.1:c.6449A=	XP_016883033.1:p.Gln2150=
XM_017027545.1:c.5885A=	XP_016883034.1:p.Gln1962=
XM_017027546.1:c.3413A=	XP_016883035.1:p.Gln1138=
NM_014727.3:c.6449A= MANE Select	NP_055542.1:p.Gln2150=