Canonical Allele Identifier: CA507308842

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733185-A-G
• MyVariant Identifiers: chr19:g.36224086A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733185A>G , CM000681.2:g.35733185A>G	GRCh38
NC_000019.9:g.36224086A>G , CM000681.1:g.36224086A>G	GRCh37
NC_000019.8:g.40915926A>G	NCBI36
NG_052906.1:g.20167A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.942A>G
ENST00000673918.2:c.6570A>G	ENSP00000501283.1:p.Pro2190=
ENST00000674114.2:c.4177A>G	ENSP00000501039.2:n.4177A>G
ENST00000684977.1:c.1854A>G	ENSP00000509384.1:p.Pro618=
ENST00000689544.1:n.1789A>G
ENST00000691421.1:c.1857A>G	ENSP00000508674.1:p.Pro619=
ENST00000691855.1:c.6178A>G
ENST00000692961.1:c.6636A>G	ENSP00000509289.1:p.Pro2212=
ENST00000693677.1:c.705-412A>G	ENSP00000509779.1:n.705-412A>G
ENST00000420124.4:c.6636A>G MANE Select	ENSP00000398837.2:p.Pro2212=
ENST00000673918.1:c.6570A>G	ENSP00000501283.1:p.Pro2190=
ENST00000674114.1:c.3958A>G
ENST00000420124.2:c.6636A>G	ENSP00000398837.1:p.Pro2212=
NM_014727.2:c.6636A>G	NP_055542.1:p.Pro2212=
XM_011527561.1:c.6570A>G	XP_011525863.1:p.Pro2190=
XM_011527562.1:c.6636A>G	XP_011525864.1:p.Pro2212=
XM_011527563.1:c.6360A>G	XP_011525865.1:p.Pro2120=
XM_011527561.2:c.6072A>G	XP_011525863.2:p.Pro2024=
XM_011527562.2:c.6636A>G	XP_011525864.1:p.Pro2212=
XM_017027544.1:c.6636A>G	XP_016883033.1:p.Pro2212=
XM_017027545.1:c.6072A>G	XP_016883034.1:p.Pro2024=
XM_017027546.1:c.3600A>G	XP_016883035.1:p.Pro1200=
NM_014727.3:c.6636A>G MANE Select	NP_055542.1:p.Pro2212=