Canonical Allele Identifier: CA2333794340

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732474A= , CM000681.2:g.35732474A=	GRCh38
NC_000019.9:g.36223375A= , CM000681.1:g.36223375A=	GRCh37
NC_000019.8:g.40915215A=	NCBI36
NG_052906.1:g.19456A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.231A=
ENST00000673918.2:c.5859A=	ENSP00000501283.1:p.Pro1953=
ENST00000674114.2:c.3466A=	ENSP00000501039.2:n.3466A=
ENST00000684977.1:c.1143A=	ENSP00000509384.1:p.Pro381=
ENST00000689544.1:n.1078A=
ENST00000691421.1:c.1146A=	ENSP00000508674.1:p.Pro382=
ENST00000691855.1:c.5467A=
ENST00000692961.1:c.5925A=	ENSP00000509289.1:p.Pro1975=
ENST00000693677.1:c.704+145A=	ENSP00000509779.1:n.704+145A=
ENST00000420124.4:c.5925A= MANE Select	ENSP00000398837.2:p.Pro1975=
ENST00000673918.1:c.5859A=	ENSP00000501283.1:p.Pro1953=
ENST00000674114.1:c.3247A=
ENST00000420124.2:c.5925A=	ENSP00000398837.1:p.Pro1975=
NM_014727.2:c.5925A=	NP_055542.1:p.Pro1975=
XM_011527561.1:c.5859A=	XP_011525863.1:p.Pro1953=
XM_011527562.1:c.5925A=	XP_011525864.1:p.Pro1975=
XM_011527563.1:c.5649A=	XP_011525865.1:p.Pro1883=
XM_011527561.2:c.5361A=	XP_011525863.2:p.Pro1787=
XM_011527562.2:c.5925A=	XP_011525864.1:p.Pro1975=
XM_017027544.1:c.5925A=	XP_016883033.1:p.Pro1975=
XM_017027545.1:c.5361A=	XP_016883034.1:p.Pro1787=
XM_017027546.1:c.2889A=	XP_016883035.1:p.Pro963=
NM_014727.3:c.5925A= MANE Select	NP_055542.1:p.Pro1975=