Canonical Allele Identifier: CA2333794445

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732687T= , CM000681.2:g.35732687T=	GRCh38
NC_000019.9:g.36223588T= , CM000681.1:g.36223588T=	GRCh37
NC_000019.8:g.40915428T=	NCBI36
NG_052906.1:g.19669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.444T=
ENST00000673918.2:c.6072T=	ENSP00000501283.1:p.Gly2024=
ENST00000674114.2:c.3679T=	ENSP00000501039.2:n.3679T=
ENST00000684977.1:c.1356T=	ENSP00000509384.1:p.Gly452=
ENST00000689544.1:n.1291T=
ENST00000691421.1:c.1359T=	ENSP00000508674.1:p.Gly453=
ENST00000691855.1:c.5680T=
ENST00000692961.1:c.6138T=	ENSP00000509289.1:p.Gly2046=
ENST00000693677.1:c.704+358T=	ENSP00000509779.1:n.704+358T=
ENST00000420124.4:c.6138T= MANE Select	ENSP00000398837.2:p.Gly2046=
ENST00000673918.1:c.6072T=	ENSP00000501283.1:p.Gly2024=
ENST00000674114.1:c.3460T=
ENST00000420124.2:c.6138T=	ENSP00000398837.1:p.Gly2046=
NM_014727.2:c.6138T=	NP_055542.1:p.Gly2046=
XM_011527561.1:c.6072T=	XP_011525863.1:p.Gly2024=
XM_011527562.1:c.6138T=	XP_011525864.1:p.Gly2046=
XM_011527563.1:c.5862T=	XP_011525865.1:p.Gly1954=
XM_011527561.2:c.5574T=	XP_011525863.2:p.Gly1858=
XM_011527562.2:c.6138T=	XP_011525864.1:p.Gly2046=
XM_017027544.1:c.6138T=	XP_016883033.1:p.Gly2046=
XM_017027545.1:c.5574T=	XP_016883034.1:p.Gly1858=
XM_017027546.1:c.3102T=	XP_016883035.1:p.Gly1034=
NM_014727.3:c.6138T= MANE Select	NP_055542.1:p.Gly2046=