Canonical Allele Identifier: CA405424667

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732488-T-G
• MyVariant Identifiers: chr19:g.36223389T>G (hg19) ; chr19:g.35732488T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732488T>G , CM000681.2:g.35732488T>G	GRCh38
NC_000019.9:g.36223389T>G , CM000681.1:g.36223389T>G	GRCh37
NC_000019.8:g.40915229T>G	NCBI36
NG_052906.1:g.19470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.245T>G
ENST00000673918.2:c.5873T>G	ENSP00000501283.1:p.Met1958Arg
ENST00000674114.2:c.3480T>G	ENSP00000501039.2:n.3480T>G
ENST00000684977.1:c.1157T>G	ENSP00000509384.1:p.Met386Arg
ENST00000689544.1:n.1092T>G
ENST00000691421.1:c.1160T>G	ENSP00000508674.1:p.Met387Arg
ENST00000691855.1:c.5481T>G
ENST00000692961.1:c.5939T>G	ENSP00000509289.1:p.Met1980Arg
ENST00000693677.1:c.704+159T>G	ENSP00000509779.1:n.704+159T>G
ENST00000420124.4:c.5939T>G MANE Select	ENSP00000398837.2:p.Met1980Arg
ENST00000673918.1:c.5873T>G	ENSP00000501283.1:p.Met1958Arg
ENST00000674114.1:c.3261T>G
ENST00000420124.2:c.5939T>G	ENSP00000398837.1:p.Met1980Arg
NM_014727.2:c.5939T>G	NP_055542.1:p.Met1980Arg
XM_011527561.1:c.5873T>G	XP_011525863.1:p.Met1958Arg
XM_011527562.1:c.5939T>G	XP_011525864.1:p.Met1980Arg
XM_011527563.1:c.5663T>G	XP_011525865.1:p.Met1888Arg
XM_011527561.2:c.5375T>G	XP_011525863.2:p.Met1792Arg
XM_011527562.2:c.5939T>G	XP_011525864.1:p.Met1980Arg
XM_017027544.1:c.5939T>G	XP_016883033.1:p.Met1980Arg
XM_017027545.1:c.5375T>G	XP_016883034.1:p.Met1792Arg
XM_017027546.1:c.2903T>G	XP_016883035.1:p.Met968Arg
NM_014727.3:c.5939T>G MANE Select	NP_055542.1:p.Met1980Arg