Canonical Allele Identifier: CA405428138

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223829G>A (hg19) ; chr19:g.35732928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732928G>A , CM000681.2:g.35732928G>A	GRCh38
NC_000019.9:g.36223829G>A , CM000681.1:g.36223829G>A	GRCh37
NC_000019.8:g.40915669G>A	NCBI36
NG_052906.1:g.19910G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.685G>A
ENST00000673918.2:c.6313G>A	ENSP00000501283.1:p.Gly2105Arg
ENST00000674114.2:c.3920G>A	ENSP00000501039.2:n.3920G>A
ENST00000684977.1:c.1597G>A	ENSP00000509384.1:p.Gly533Arg
ENST00000689544.1:n.1532G>A
ENST00000691421.1:c.1600G>A	ENSP00000508674.1:p.Gly534Arg
ENST00000691855.1:c.5921G>A
ENST00000692961.1:c.6379G>A	ENSP00000509289.1:p.Gly2127Arg
ENST00000693677.1:c.704+599G>A	ENSP00000509779.1:n.704+599G>A
ENST00000420124.4:c.6379G>A MANE Select	ENSP00000398837.2:p.Gly2127Arg
ENST00000673918.1:c.6313G>A	ENSP00000501283.1:p.Gly2105Arg
ENST00000674114.1:c.3701G>A
ENST00000420124.2:c.6379G>A	ENSP00000398837.1:p.Gly2127Arg
NM_014727.2:c.6379G>A	NP_055542.1:p.Gly2127Arg
XM_011527561.1:c.6313G>A	XP_011525863.1:p.Gly2105Arg
XM_011527562.1:c.6379G>A	XP_011525864.1:p.Gly2127Arg
XM_011527563.1:c.6103G>A	XP_011525865.1:p.Gly2035Arg
XM_011527561.2:c.5815G>A	XP_011525863.2:p.Gly1939Arg
XM_011527562.2:c.6379G>A	XP_011525864.1:p.Gly2127Arg
XM_017027544.1:c.6379G>A	XP_016883033.1:p.Gly2127Arg
XM_017027545.1:c.5815G>A	XP_016883034.1:p.Gly1939Arg
XM_017027546.1:c.3343G>A	XP_016883035.1:p.Gly1115Arg
NM_014727.3:c.6379G>A MANE Select	NP_055542.1:p.Gly2127Arg