Canonical Allele Identifier: CA2333794674

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733125A= , CM000681.2:g.35733125A=	GRCh38
NC_000019.9:g.36224026A= , CM000681.1:g.36224026A=	GRCh37
NC_000019.8:g.40915866A=	NCBI36
NG_052906.1:g.20107A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.882A=
ENST00000673918.2:c.6510A=	ENSP00000501283.1:p.Ile2170=
ENST00000674114.2:c.4117A=	ENSP00000501039.2:n.4117A=
ENST00000684977.1:c.1794A=	ENSP00000509384.1:p.Ile598=
ENST00000689544.1:n.1729A=
ENST00000691421.1:c.1797A=	ENSP00000508674.1:p.Ile599=
ENST00000691855.1:c.6118A=
ENST00000692961.1:c.6576A=	ENSP00000509289.1:p.Ile2192=
ENST00000693677.1:c.705-472A=	ENSP00000509779.1:n.705-472A=
ENST00000420124.4:c.6576A= MANE Select	ENSP00000398837.2:p.Ile2192=
ENST00000673918.1:c.6510A=	ENSP00000501283.1:p.Ile2170=
ENST00000674114.1:c.3898A=
ENST00000420124.2:c.6576A=	ENSP00000398837.1:p.Ile2192=
NM_014727.2:c.6576A=	NP_055542.1:p.Ile2192=
XM_011527561.1:c.6510A=	XP_011525863.1:p.Ile2170=
XM_011527562.1:c.6576A=	XP_011525864.1:p.Ile2192=
XM_011527563.1:c.6300A=	XP_011525865.1:p.Ile2100=
XM_011527561.2:c.6012A=	XP_011525863.2:p.Ile2004=
XM_011527562.2:c.6576A=	XP_011525864.1:p.Ile2192=
XM_017027544.1:c.6576A=	XP_016883033.1:p.Ile2192=
XM_017027545.1:c.6012A=	XP_016883034.1:p.Ile2004=
XM_017027546.1:c.3540A=	XP_016883035.1:p.Ile1180=
NM_014727.3:c.6576A= MANE Select	NP_055542.1:p.Ile2192=