Canonical Allele Identifier: CA2333794390

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732599A= , CM000681.2:g.35732599A=	GRCh38
NC_000019.9:g.36223500A= , CM000681.1:g.36223500A=	GRCh37
NC_000019.8:g.40915340A=	NCBI36
NG_052906.1:g.19581A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.356A=
ENST00000673918.2:c.5984A=	ENSP00000501283.1:p.His1995=
ENST00000674114.2:c.3591A=	ENSP00000501039.2:n.3591A=
ENST00000684977.1:c.1268A=	ENSP00000509384.1:p.His423=
ENST00000689544.1:n.1203A=
ENST00000691421.1:c.1271A=	ENSP00000508674.1:p.His424=
ENST00000691855.1:c.5592A=
ENST00000692961.1:c.6050A=	ENSP00000509289.1:p.His2017=
ENST00000693677.1:c.704+270A=	ENSP00000509779.1:n.704+270A=
ENST00000420124.4:c.6050A= MANE Select	ENSP00000398837.2:p.His2017=
ENST00000673918.1:c.5984A=	ENSP00000501283.1:p.His1995=
ENST00000674114.1:c.3372A=
ENST00000420124.2:c.6050A=	ENSP00000398837.1:p.His2017=
NM_014727.2:c.6050A=	NP_055542.1:p.His2017=
XM_011527561.1:c.5984A=	XP_011525863.1:p.His1995=
XM_011527562.1:c.6050A=	XP_011525864.1:p.His2017=
XM_011527563.1:c.5774A=	XP_011525865.1:p.His1925=
XM_011527561.2:c.5486A=	XP_011525863.2:p.His1829=
XM_011527562.2:c.6050A=	XP_011525864.1:p.His2017=
XM_017027544.1:c.6050A=	XP_016883033.1:p.His2017=
XM_017027545.1:c.5486A=	XP_016883034.1:p.His1829=
XM_017027546.1:c.3014A=	XP_016883035.1:p.His1005=
NM_014727.3:c.6050A= MANE Select	NP_055542.1:p.His2017=