Canonical Allele Identifier: CA2333793122

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730123A= , CM000681.2:g.35730123A=	GRCh38
NC_000019.9:g.36221024A= , CM000681.1:g.36221024A=	GRCh37
NC_000019.8:g.40912864A=	NCBI36
NG_052906.1:g.17105A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.5008A=	ENSP00000501283.1:p.Lys1670=
ENST00000674114.2:c.2615A=	ENSP00000501039.2:n.2615A=
ENST00000684977.1:c.292A=	ENSP00000509384.1:p.Lys98=
ENST00000685168.1:c.500A=
ENST00000689544.1:n.227A=
ENST00000691421.1:c.295A=	ENSP00000508674.1:p.Lys99=
ENST00000691855.1:c.4616A=
ENST00000692961.1:c.5074A=	ENSP00000509289.1:p.Lys1692=
ENST00000420124.4:c.5074A= MANE Select	ENSP00000398837.2:p.Lys1692=
ENST00000673918.1:c.5008A=	ENSP00000501283.1:p.Lys1670=
ENST00000674114.1:c.2396A=
ENST00000420124.2:c.5074A=	ENSP00000398837.1:p.Lys1692=
NM_014727.2:c.5074A=	NP_055542.1:p.Lys1692=
XM_011527561.1:c.5008A=	XP_011525863.1:p.Lys1670=
XM_011527562.1:c.5074A=	XP_011525864.1:p.Lys1692=
XM_011527563.1:c.4798A=	XP_011525865.1:p.Lys1600=
XM_011527561.2:c.4510A=	XP_011525863.2:p.Lys1504=
XM_011527562.2:c.5074A=	XP_011525864.1:p.Lys1692=
XM_017027544.1:c.5074A=	XP_016883033.1:p.Lys1692=
XM_017027545.1:c.4510A=	XP_016883034.1:p.Lys1504=
XM_017027546.1:c.2038A=	XP_016883035.1:p.Lys680=
NM_014727.3:c.5074A= MANE Select	NP_055542.1:p.Lys1692=