Canonical Allele Identifier: CA2333793101

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730057A= , CM000681.2:g.35730057A=	GRCh38
NC_000019.9:g.36220958A= , CM000681.1:g.36220958A=	GRCh37
NC_000019.8:g.40912798A=	NCBI36
NG_052906.1:g.17039A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4942A=	ENSP00000501283.1:p.Ser1648=
ENST00000674114.2:c.2549A=	ENSP00000501039.2:n.2549A=
ENST00000684977.1:c.226A=	ENSP00000509384.1:p.Ser76=
ENST00000685168.1:c.434A=
ENST00000689544.1:n.161A=
ENST00000691421.1:c.229A=	ENSP00000508674.1:p.Ser77=
ENST00000691855.1:c.4550A=
ENST00000692961.1:c.5008A=	ENSP00000509289.1:p.Ser1670=
ENST00000420124.4:c.5008A= MANE Select	ENSP00000398837.2:p.Ser1670=
ENST00000673918.1:c.4942A=	ENSP00000501283.1:p.Ser1648=
ENST00000674114.1:c.2330A=
ENST00000420124.2:c.5008A=	ENSP00000398837.1:p.Ser1670=
NM_014727.2:c.5008A=	NP_055542.1:p.Ser1670=
XM_011527561.1:c.4942A=	XP_011525863.1:p.Ser1648=
XM_011527562.1:c.5008A=	XP_011525864.1:p.Ser1670=
XM_011527563.1:c.4732A=	XP_011525865.1:p.Ser1578=
XM_011527561.2:c.4444A=	XP_011525863.2:p.Ser1482=
XM_011527562.2:c.5008A=	XP_011525864.1:p.Ser1670=
XM_017027544.1:c.5008A=	XP_016883033.1:p.Ser1670=
XM_017027545.1:c.4444A=	XP_016883034.1:p.Ser1482=
XM_017027546.1:c.1972A=	XP_016883035.1:p.Ser658=
NM_014727.3:c.5008A= MANE Select	NP_055542.1:p.Ser1670=