Canonical Allele Identifier: CA507073812

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733820-C-G
• MyVariant Identifiers: chr19:g.36224721C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733820C>G , CM000681.2:g.35733820C>G	GRCh38
NC_000019.9:g.36224721C>G , CM000681.1:g.36224721C>G	GRCh37
NC_000019.8:g.40916561C>G	NCBI36
NG_052906.1:g.20802C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.1577C>G
ENST00000673918.2:c.7041C>G	ENSP00000501283.1:p.Val2347=
ENST00000674114.2:c.4648C>G	ENSP00000501039.2:n.4648C>G
ENST00000684977.1:c.2302C>G	ENSP00000509384.1:n.2302C>G
ENST00000689544.1:n.2348C>G
ENST00000689929.1:c.58C>G
ENST00000691421.1:c.2238C>G	ENSP00000508674.1:p.Val746=
ENST00000691855.1:c.6649C>G
ENST00000692961.1:c.7031C>G	ENSP00000509289.1:p.Ser2344Cys
ENST00000693175.1:c.58C>G
ENST00000693677.1:c.852C>G	ENSP00000509779.1:p.Val284=
ENST00000420124.4:c.7107C>G MANE Select	ENSP00000398837.2:p.Val2369=
ENST00000673918.1:c.7041C>G	ENSP00000501283.1:p.Val2347=
ENST00000674114.1:c.4429C>G
ENST00000420124.2:c.7107C>G	ENSP00000398837.1:p.Val2369=
ENST00000592092.1:n.487C>G
NM_014727.2:c.7107C>G	NP_055542.1:p.Val2369=
XM_011527561.1:c.7041C>G	XP_011525863.1:p.Val2347=
XM_011527562.1:c.7107C>G	XP_011525864.1:p.Val2369=
XM_011527563.1:c.6831C>G	XP_011525865.1:p.Val2277=
XM_011527561.2:c.6543C>G	XP_011525863.2:p.Val2181=
XM_011527562.2:c.7107C>G	XP_011525864.1:p.Val2369=
XM_017027544.1:c.7017C>G	XP_016883033.1:p.Val2339=
XM_017027545.1:c.6543C>G	XP_016883034.1:p.Val2181=
XM_017027546.1:c.4071C>G	XP_016883035.1:p.Val1357=
NM_014727.3:c.7107C>G MANE Select	NP_055542.1:p.Val2369=