Canonical Allele Identifier: CA2333794580

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732960C= , CM000681.2:g.35732960C=	GRCh38
NC_000019.9:g.36223861C= , CM000681.1:g.36223861C=	GRCh37
NC_000019.8:g.40915701C=	NCBI36
NG_052906.1:g.19942C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.717C=
ENST00000673918.2:c.6345C=	ENSP00000501283.1:p.Pro2115=
ENST00000674114.2:c.3952C=	ENSP00000501039.2:n.3952C=
ENST00000684977.1:c.1629C=	ENSP00000509384.1:p.Pro543=
ENST00000689544.1:n.1564C=
ENST00000691421.1:c.1632C=	ENSP00000508674.1:p.Pro544=
ENST00000691855.1:c.5953C=
ENST00000692961.1:c.6411C=	ENSP00000509289.1:p.Pro2137=
ENST00000693677.1:c.704+631C=	ENSP00000509779.1:n.704+631C=
ENST00000420124.4:c.6411C= MANE Select	ENSP00000398837.2:p.Pro2137=
ENST00000673918.1:c.6345C=	ENSP00000501283.1:p.Pro2115=
ENST00000674114.1:c.3733C=
ENST00000420124.2:c.6411C=	ENSP00000398837.1:p.Pro2137=
NM_014727.2:c.6411C=	NP_055542.1:p.Pro2137=
XM_011527561.1:c.6345C=	XP_011525863.1:p.Pro2115=
XM_011527562.1:c.6411C=	XP_011525864.1:p.Pro2137=
XM_011527563.1:c.6135C=	XP_011525865.1:p.Pro2045=
XM_011527561.2:c.5847C=	XP_011525863.2:p.Pro1949=
XM_011527562.2:c.6411C=	XP_011525864.1:p.Pro2137=
XM_017027544.1:c.6411C=	XP_016883033.1:p.Pro2137=
XM_017027545.1:c.5847C=	XP_016883034.1:p.Pro1949=
XM_017027546.1:c.3375C=	XP_016883035.1:p.Pro1125=
NM_014727.3:c.6411C= MANE Select	NP_055542.1:p.Pro2137=