Canonical Allele Identifier: CA2333794321

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732441C= , CM000681.2:g.35732441C=	GRCh38
NC_000019.9:g.36223342C= , CM000681.1:g.36223342C=	GRCh37
NC_000019.8:g.40915182C=	NCBI36
NG_052906.1:g.19423C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.198C=
ENST00000673918.2:c.5826C=	ENSP00000501283.1:p.Ala1942=
ENST00000674114.2:c.3433C=	ENSP00000501039.2:n.3433C=
ENST00000684977.1:c.1110C=	ENSP00000509384.1:p.Ala370=
ENST00000689544.1:n.1045C=
ENST00000691421.1:c.1113C=	ENSP00000508674.1:p.Ala371=
ENST00000691855.1:c.5434C=
ENST00000692961.1:c.5892C=	ENSP00000509289.1:p.Ala1964=
ENST00000693677.1:c.704+112C=	ENSP00000509779.1:n.704+112C=
ENST00000420124.4:c.5892C= MANE Select	ENSP00000398837.2:p.Ala1964=
ENST00000673918.1:c.5826C=	ENSP00000501283.1:p.Ala1942=
ENST00000674114.1:c.3214C=
ENST00000420124.2:c.5892C=	ENSP00000398837.1:p.Ala1964=
NM_014727.2:c.5892C=	NP_055542.1:p.Ala1964=
XM_011527561.1:c.5826C=	XP_011525863.1:p.Ala1942=
XM_011527562.1:c.5892C=	XP_011525864.1:p.Ala1964=
XM_011527563.1:c.5616C=	XP_011525865.1:p.Ala1872=
XM_011527561.2:c.5328C=	XP_011525863.2:p.Ala1776=
XM_011527562.2:c.5892C=	XP_011525864.1:p.Ala1964=
XM_017027544.1:c.5892C=	XP_016883033.1:p.Ala1964=
XM_017027545.1:c.5328C=	XP_016883034.1:p.Ala1776=
XM_017027546.1:c.2856C=	XP_016883035.1:p.Ala952=
NM_014727.3:c.5892C= MANE Select	NP_055542.1:p.Ala1964=