Canonical Allele Identifier: CA2333794568

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732933T= , CM000681.2:g.35732933T=	GRCh38
NC_000019.9:g.36223834T= , CM000681.1:g.36223834T=	GRCh37
NC_000019.8:g.40915674T=	NCBI36
NG_052906.1:g.19915T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.690T=
ENST00000673918.2:c.6318T=	ENSP00000501283.1:p.Gly2106=
ENST00000674114.2:c.3925T=	ENSP00000501039.2:n.3925T=
ENST00000684977.1:c.1602T=	ENSP00000509384.1:p.Gly534=
ENST00000689544.1:n.1537T=
ENST00000691421.1:c.1605T=	ENSP00000508674.1:p.Gly535=
ENST00000691855.1:c.5926T=
ENST00000692961.1:c.6384T=	ENSP00000509289.1:p.Gly2128=
ENST00000693677.1:c.704+604T=	ENSP00000509779.1:n.704+604T=
ENST00000420124.4:c.6384T= MANE Select	ENSP00000398837.2:p.Gly2128=
ENST00000673918.1:c.6318T=	ENSP00000501283.1:p.Gly2106=
ENST00000674114.1:c.3706T=
ENST00000420124.2:c.6384T=	ENSP00000398837.1:p.Gly2128=
NM_014727.2:c.6384T=	NP_055542.1:p.Gly2128=
XM_011527561.1:c.6318T=	XP_011525863.1:p.Gly2106=
XM_011527562.1:c.6384T=	XP_011525864.1:p.Gly2128=
XM_011527563.1:c.6108T=	XP_011525865.1:p.Gly2036=
XM_011527561.2:c.5820T=	XP_011525863.2:p.Gly1940=
XM_011527562.2:c.6384T=	XP_011525864.1:p.Gly2128=
XM_017027544.1:c.6384T=	XP_016883033.1:p.Gly2128=
XM_017027545.1:c.5820T=	XP_016883034.1:p.Gly1940=
XM_017027546.1:c.3348T=	XP_016883035.1:p.Gly1116=
NM_014727.3:c.6384T= MANE Select	NP_055542.1:p.Gly2128=