Canonical Allele Identifier: CA507308441

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732855-G-A
• MyVariant Identifiers: chr19:g.36223756G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732855G>A , CM000681.2:g.35732855G>A	GRCh38
NC_000019.9:g.36223756G>A , CM000681.1:g.36223756G>A	GRCh37
NC_000019.8:g.40915596G>A	NCBI36
NG_052906.1:g.19837G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.612G>A
ENST00000673918.2:c.6240G>A	ENSP00000501283.1:p.Arg2080=
ENST00000674114.2:c.3847G>A	ENSP00000501039.2:n.3847G>A
ENST00000684977.1:c.1524G>A	ENSP00000509384.1:p.Arg508=
ENST00000689544.1:n.1459G>A
ENST00000691421.1:c.1527G>A	ENSP00000508674.1:p.Arg509=
ENST00000691855.1:c.5848G>A
ENST00000692961.1:c.6306G>A	ENSP00000509289.1:p.Arg2102=
ENST00000693677.1:c.704+526G>A	ENSP00000509779.1:n.704+526G>A
ENST00000420124.4:c.6306G>A MANE Select	ENSP00000398837.2:p.Arg2102=
ENST00000673918.1:c.6240G>A	ENSP00000501283.1:p.Arg2080=
ENST00000674114.1:c.3628G>A
ENST00000420124.2:c.6306G>A	ENSP00000398837.1:p.Arg2102=
NM_014727.2:c.6306G>A	NP_055542.1:p.Arg2102=
XM_011527561.1:c.6240G>A	XP_011525863.1:p.Arg2080=
XM_011527562.1:c.6306G>A	XP_011525864.1:p.Arg2102=
XM_011527563.1:c.6030G>A	XP_011525865.1:p.Arg2010=
XM_011527561.2:c.5742G>A	XP_011525863.2:p.Arg1914=
XM_011527562.2:c.6306G>A	XP_011525864.1:p.Arg2102=
XM_017027544.1:c.6306G>A	XP_016883033.1:p.Arg2102=
XM_017027545.1:c.5742G>A	XP_016883034.1:p.Arg1914=
XM_017027546.1:c.3270G>A	XP_016883035.1:p.Arg1090=
NM_014727.3:c.6306G>A MANE Select	NP_055542.1:p.Arg2102=