Canonical Allele Identifier: CA507308794

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224670C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733769C>G , CM000681.2:g.35733769C>G	GRCh38
NC_000019.9:g.36224670C>G , CM000681.1:g.36224670C>G	GRCh37
NC_000019.8:g.40916510C>G	NCBI36
NG_052906.1:g.20751C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.1526C>G
ENST00000673918.2:c.6990C>G	ENSP00000501283.1:p.Leu2330=
ENST00000674114.2:c.4597C>G	ENSP00000501039.2:n.4597C>G
ENST00000684977.1:c.2251C>G	ENSP00000509384.1:n.2251C>G
ENST00000689544.1:n.2297C>G
ENST00000689929.1:c.7C>G
ENST00000691421.1:c.2187C>G	ENSP00000508674.1:p.Leu729=
ENST00000691855.1:c.6598C>G
ENST00000692961.1:c.6980C>G	ENSP00000509289.1:p.Ser2327Cys
ENST00000693175.1:c.7C>G
ENST00000693677.1:c.801C>G	ENSP00000509779.1:p.Leu267=
ENST00000420124.4:c.7056C>G MANE Select	ENSP00000398837.2:p.Leu2352=
ENST00000673918.1:c.6990C>G	ENSP00000501283.1:p.Leu2330=
ENST00000674114.1:c.4378C>G
ENST00000420124.2:c.7056C>G	ENSP00000398837.1:p.Leu2352=
ENST00000592092.1:n.436C>G
NM_014727.2:c.7056C>G	NP_055542.1:p.Leu2352=
XM_011527561.1:c.6990C>G	XP_011525863.1:p.Leu2330=
XM_011527562.1:c.7056C>G	XP_011525864.1:p.Leu2352=
XM_011527563.1:c.6780C>G	XP_011525865.1:p.Leu2260=
XM_011527561.2:c.6492C>G	XP_011525863.2:p.Leu2164=
XM_011527562.2:c.7056C>G	XP_011525864.1:p.Leu2352=
XM_017027544.1:c.6966C>G	XP_016883033.1:p.Leu2322=
XM_017027545.1:c.6492C>G	XP_016883034.1:p.Leu2164=
XM_017027546.1:c.4020C>G	XP_016883035.1:p.Leu1340=
NM_014727.3:c.7056C>G MANE Select	NP_055542.1:p.Leu2352=