Canonical Allele Identifier: CA507072537

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220906C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730005C>A , CM000681.2:g.35730005C>A	GRCh38
NC_000019.9:g.36220906C>A , CM000681.1:g.36220906C>A	GRCh37
NC_000019.8:g.40912746C>A	NCBI36
NG_052906.1:g.16987C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4890C>A	ENSP00000501283.1:p.Gly1630=
ENST00000674114.2:c.2497C>A	ENSP00000501039.2:n.2497C>A
ENST00000684977.1:c.174C>A	ENSP00000509384.1:p.Gly58=
ENST00000685168.1:c.382C>A
ENST00000689544.1:n.109C>A
ENST00000691421.1:c.177C>A	ENSP00000508674.1:p.Gly59=
ENST00000691855.1:c.4498C>A
ENST00000692961.1:c.4956C>A	ENSP00000509289.1:p.Gly1652=
ENST00000420124.4:c.4956C>A MANE Select	ENSP00000398837.2:p.Gly1652=
ENST00000673918.1:c.4890C>A	ENSP00000501283.1:p.Gly1630=
ENST00000674114.1:c.2278C>A
ENST00000420124.2:c.4956C>A	ENSP00000398837.1:p.Gly1652=
NM_014727.2:c.4956C>A	NP_055542.1:p.Gly1652=
XM_011527561.1:c.4890C>A	XP_011525863.1:p.Gly1630=
XM_011527562.1:c.4956C>A	XP_011525864.1:p.Gly1652=
XM_011527563.1:c.4680C>A	XP_011525865.1:p.Gly1560=
XM_011527561.2:c.4392C>A	XP_011525863.2:p.Gly1464=
XM_011527562.2:c.4956C>A	XP_011525864.1:p.Gly1652=
XM_017027544.1:c.4956C>A	XP_016883033.1:p.Gly1652=
XM_017027545.1:c.4392C>A	XP_016883034.1:p.Gly1464=
XM_017027546.1:c.1920C>A	XP_016883035.1:p.Gly640=
NM_014727.3:c.4956C>A MANE Select	NP_055542.1:p.Gly1652=