Canonical Allele Identifier: CA507308831

Gene: KMT2B

Linked Data

• dbSNP Id: rs1969769241
• MyVariant Identifiers: chr19:g.36223858C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732957C>G , CM000681.2:g.35732957C>G	GRCh38
NC_000019.9:g.36223858C>G , CM000681.1:g.36223858C>G	GRCh37
NC_000019.8:g.40915698C>G	NCBI36
NG_052906.1:g.19939C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.714C>G
ENST00000673918.2:c.6342C>G	ENSP00000501283.1:p.Leu2114=
ENST00000674114.2:c.3949C>G	ENSP00000501039.2:n.3949C>G
ENST00000684977.1:c.1626C>G	ENSP00000509384.1:p.Leu542=
ENST00000689544.1:n.1561C>G
ENST00000691421.1:c.1629C>G	ENSP00000508674.1:p.Leu543=
ENST00000691855.1:c.5950C>G
ENST00000692961.1:c.6408C>G	ENSP00000509289.1:p.Leu2136=
ENST00000693677.1:c.704+628C>G	ENSP00000509779.1:n.704+628C>G
ENST00000420124.4:c.6408C>G MANE Select	ENSP00000398837.2:p.Leu2136=
ENST00000673918.1:c.6342C>G	ENSP00000501283.1:p.Leu2114=
ENST00000674114.1:c.3730C>G
ENST00000420124.2:c.6408C>G	ENSP00000398837.1:p.Leu2136=
NM_014727.2:c.6408C>G	NP_055542.1:p.Leu2136=
XM_011527561.1:c.6342C>G	XP_011525863.1:p.Leu2114=
XM_011527562.1:c.6408C>G	XP_011525864.1:p.Leu2136=
XM_011527563.1:c.6132C>G	XP_011525865.1:p.Leu2044=
XM_011527561.2:c.5844C>G	XP_011525863.2:p.Leu1948=
XM_011527562.2:c.6408C>G	XP_011525864.1:p.Leu2136=
XM_017027544.1:c.6408C>G	XP_016883033.1:p.Leu2136=
XM_017027545.1:c.5844C>G	XP_016883034.1:p.Leu1948=
XM_017027546.1:c.3372C>G	XP_016883035.1:p.Leu1124=
NM_014727.3:c.6408C>G MANE Select	NP_055542.1:p.Leu2136=