Canonical Allele Identifier: CA2333794612

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733020T= , CM000681.2:g.35733020T=	GRCh38
NC_000019.9:g.36223921T= , CM000681.1:g.36223921T=	GRCh37
NC_000019.8:g.40915761T=	NCBI36
NG_052906.1:g.20002T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.777T=
ENST00000673918.2:c.6405T=	ENSP00000501283.1:p.Ala2135=
ENST00000674114.2:c.4012T=	ENSP00000501039.2:n.4012T=
ENST00000684977.1:c.1689T=	ENSP00000509384.1:p.Ala563=
ENST00000689544.1:n.1624T=
ENST00000691421.1:c.1692T=	ENSP00000508674.1:p.Ala564=
ENST00000691855.1:c.6013T=
ENST00000692961.1:c.6471T=	ENSP00000509289.1:p.Ala2157=
ENST00000693677.1:c.705-577T=	ENSP00000509779.1:n.705-577T=
ENST00000420124.4:c.6471T= MANE Select	ENSP00000398837.2:p.Ala2157=
ENST00000673918.1:c.6405T=	ENSP00000501283.1:p.Ala2135=
ENST00000674114.1:c.3793T=
ENST00000420124.2:c.6471T=	ENSP00000398837.1:p.Ala2157=
NM_014727.2:c.6471T=	NP_055542.1:p.Ala2157=
XM_011527561.1:c.6405T=	XP_011525863.1:p.Ala2135=
XM_011527562.1:c.6471T=	XP_011525864.1:p.Ala2157=
XM_011527563.1:c.6195T=	XP_011525865.1:p.Ala2065=
XM_011527561.2:c.5907T=	XP_011525863.2:p.Ala1969=
XM_011527562.2:c.6471T=	XP_011525864.1:p.Ala2157=
XM_017027544.1:c.6471T=	XP_016883033.1:p.Ala2157=
XM_017027545.1:c.5907T=	XP_016883034.1:p.Ala1969=
XM_017027546.1:c.3435T=	XP_016883035.1:p.Ala1145=
NM_014727.3:c.6471T= MANE Select	NP_055542.1:p.Ala2157=