Canonical Allele Identifier: CA507072432

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220870C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729969C>A , CM000681.2:g.35729969C>A	GRCh38
NC_000019.9:g.36220870C>A , CM000681.1:g.36220870C>A	GRCh37
NC_000019.8:g.40912710C>A	NCBI36
NG_052906.1:g.16951C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4854C>A	ENSP00000501283.1:p.Arg1618=
ENST00000674114.2:c.2461C>A	ENSP00000501039.2:n.2461C>A
ENST00000684977.1:c.138C>A	ENSP00000509384.1:p.Arg46=
ENST00000685168.1:c.346C>A
ENST00000689544.1:n.73C>A
ENST00000691421.1:c.141C>A	ENSP00000508674.1:p.Arg47=
ENST00000691855.1:c.4462C>A
ENST00000692961.1:c.4920C>A	ENSP00000509289.1:p.Arg1640=
ENST00000420124.4:c.4920C>A MANE Select	ENSP00000398837.2:p.Arg1640=
ENST00000673918.1:c.4854C>A	ENSP00000501283.1:p.Arg1618=
ENST00000674114.1:c.2242C>A
ENST00000420124.2:c.4920C>A	ENSP00000398837.1:p.Arg1640=
NM_014727.2:c.4920C>A	NP_055542.1:p.Arg1640=
XM_011527561.1:c.4854C>A	XP_011525863.1:p.Arg1618=
XM_011527562.1:c.4920C>A	XP_011525864.1:p.Arg1640=
XM_011527563.1:c.4644C>A	XP_011525865.1:p.Arg1548=
XM_011527561.2:c.4356C>A	XP_011525863.2:p.Arg1452=
XM_011527562.2:c.4920C>A	XP_011525864.1:p.Arg1640=
XM_017027544.1:c.4920C>A	XP_016883033.1:p.Arg1640=
XM_017027545.1:c.4356C>A	XP_016883034.1:p.Arg1452=
XM_017027546.1:c.1884C>A	XP_016883035.1:p.Arg628=
NM_014727.3:c.4920C>A MANE Select	NP_055542.1:p.Arg1640=