Canonical Allele Identifier: CA2333795010

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733716G= , CM000681.2:g.35733716G=	GRCh38
NC_000019.9:g.36224617G= , CM000681.1:g.36224617G=	GRCh37
NC_000019.8:g.40916457G=	NCBI36
NG_052906.1:g.20698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.1473G=
ENST00000673918.2:c.6983+30G=	ENSP00000501283.1:n.6983+30G=
ENST00000674114.2:c.4590+30G=	ENSP00000501039.2:n.4590+30G=
ENST00000684977.1:c.2244+30G=	ENSP00000509384.1:n.2244+30G=
ENST00000689544.1:n.2290+30G=
ENST00000691421.1:c.2181-47G=	ENSP00000508674.1:n.2181-47G=
ENST00000691855.1:c.6591+30G=
ENST00000692961.1:c.6960-33G=	ENSP00000509289.1:n.6960-33G=
ENST00000693677.1:c.794+30G=	ENSP00000509779.1:n.794+30G=
ENST00000420124.4:c.7049+30G= MANE Select	ENSP00000398837.2:n.7049+30G=
ENST00000673918.1:c.6983+30G=	ENSP00000501283.1:n.6983+30G=
ENST00000674114.1:c.4371+30G=
ENST00000420124.2:c.7049+30G=	ENSP00000398837.1:n.7049+30G=
ENST00000592092.1:n.429+30G=
NM_014727.2:c.7049+30G=	NP_055542.1:n.7049+30G=
XM_011527561.1:c.6983+30G=	XP_011525863.1:n.6983+30G=
XM_011527562.1:c.7049+30G=	XP_011525864.1:n.7049+30G=
XM_011527563.1:c.6773+30G=	XP_011525865.1:n.6773+30G=
XM_011527561.2:c.6485+30G=	XP_011525863.2:n.6485+30G=
XM_011527562.2:c.7049+30G=	XP_011525864.1:n.7049+30G=
XM_017027544.1:c.6960-47G=	XP_016883033.1:n.6960-47G=
XM_017027545.1:c.6485+30G=	XP_016883034.1:n.6485+30G=
XM_017027546.1:c.4013+30G=	XP_016883035.1:n.4013+30G=
NM_014727.3:c.7049+30G= MANE Select	NP_055542.1:n.7049+30G=