Canonical Allele Identifier: CA307796221

Gene: KMT2B

Linked Data

• dbSNP Id: rs774512936
• gnomAD v2: 19-36223512-G-A
• gnomAD v4: 19-35732611-G-A
• MyVariant Identifiers: chr19:g.36223512G>A (hg19) ; chr19:g.35732611G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732611G>A , CM000681.2:g.35732611G>A	GRCh38
NC_000019.9:g.36223512G>A , CM000681.1:g.36223512G>A	GRCh37
NC_000019.8:g.40915352G>A	NCBI36
NG_052906.1:g.19593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.368G>A
ENST00000673918.2:c.5996G>A	ENSP00000501283.1:p.Gly1999Glu
ENST00000674114.2:c.3603G>A	ENSP00000501039.2:n.3603G>A
ENST00000684977.1:c.1280G>A	ENSP00000509384.1:p.Gly427Glu
ENST00000689544.1:n.1215G>A
ENST00000691421.1:c.1283G>A	ENSP00000508674.1:p.Gly428Glu
ENST00000691855.1:c.5604G>A
ENST00000692961.1:c.6062G>A	ENSP00000509289.1:p.Gly2021Glu
ENST00000693677.1:c.704+282G>A	ENSP00000509779.1:n.704+282G>A
ENST00000420124.4:c.6062G>A MANE Select	ENSP00000398837.2:p.Gly2021Glu
ENST00000673918.1:c.5996G>A	ENSP00000501283.1:p.Gly1999Glu
ENST00000674114.1:c.3384G>A
ENST00000420124.2:c.6062G>A	ENSP00000398837.1:p.Gly2021Glu
NM_014727.2:c.6062G>A	NP_055542.1:p.Gly2021Glu
XM_011527561.1:c.5996G>A	XP_011525863.1:p.Gly1999Glu
XM_011527562.1:c.6062G>A	XP_011525864.1:p.Gly2021Glu
XM_011527563.1:c.5786G>A	XP_011525865.1:p.Gly1929Glu
XM_011527561.2:c.5498G>A	XP_011525863.2:p.Gly1833Glu
XM_011527562.2:c.6062G>A	XP_011525864.1:p.Gly2021Glu
XM_017027544.1:c.6062G>A	XP_016883033.1:p.Gly2021Glu
XM_017027545.1:c.5498G>A	XP_016883034.1:p.Gly1833Glu
XM_017027546.1:c.3026G>A	XP_016883035.1:p.Gly1009Glu
NM_014727.3:c.6062G>A MANE Select	NP_055542.1:p.Gly2021Glu