Canonical Allele Identifier: CA2333793047

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729906G= , CM000681.2:g.35729906G=	GRCh38
NC_000019.9:g.36220807G= , CM000681.1:g.36220807G=	GRCh37
NC_000019.8:g.40912647G=	NCBI36
NG_052906.1:g.16888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4852-61G=	ENSP00000501283.1:n.4852-61G=
ENST00000674114.2:c.2459-61G=	ENSP00000501039.2:n.2459-61G=
ENST00000684977.1:c.136-61G=	ENSP00000509384.1:n.136-61G=
ENST00000685168.1:c.344-61G=
ENST00000689544.1:n.71-61G=
ENST00000691421.1:c.139-61G=	ENSP00000508674.1:n.139-61G=
ENST00000691855.1:c.4460-61G=
ENST00000692961.1:c.4918-61G=	ENSP00000509289.1:n.4918-61G=
ENST00000420124.4:c.4918-61G= MANE Select	ENSP00000398837.2:n.4918-61G=
ENST00000673918.1:c.4852-61G=	ENSP00000501283.1:n.4852-61G=
ENST00000674114.1:c.2240-61G=
ENST00000420124.2:c.4918-61G=	ENSP00000398837.1:n.4918-61G=
NM_014727.2:c.4918-61G=	NP_055542.1:n.4918-61G=
XM_011527561.1:c.4852-61G=	XP_011525863.1:n.4852-61G=
XM_011527562.1:c.4918-61G=	XP_011525864.1:n.4918-61G=
XM_011527563.1:c.4642-61G=	XP_011525865.1:n.4642-61G=
XM_011527561.2:c.4354-61G=	XP_011525863.2:n.4354-61G=
XM_011527562.2:c.4918-61G=	XP_011525864.1:n.4918-61G=
XM_017027544.1:c.4918-61G=	XP_016883033.1:n.4918-61G=
XM_017027545.1:c.4354-61G=	XP_016883034.1:n.4354-61G=
XM_017027546.1:c.1882-61G=	XP_016883035.1:n.1882-61G=
NM_014727.3:c.4918-61G= MANE Select	NP_055542.1:n.4918-61G=