Canonical Allele Identifier: CA507072671

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220969C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730068C>A , CM000681.2:g.35730068C>A	GRCh38
NC_000019.9:g.36220969C>A , CM000681.1:g.36220969C>A	GRCh37
NC_000019.8:g.40912809C>A	NCBI36
NG_052906.1:g.17050C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4953C>A	ENSP00000501283.1:p.Ile1651=
ENST00000674114.2:c.2560C>A	ENSP00000501039.2:n.2560C>A
ENST00000684977.1:c.237C>A	ENSP00000509384.1:p.Ile79=
ENST00000685168.1:c.445C>A
ENST00000689544.1:n.172C>A
ENST00000691421.1:c.240C>A	ENSP00000508674.1:p.Ile80=
ENST00000691855.1:c.4561C>A
ENST00000692961.1:c.5019C>A	ENSP00000509289.1:p.Ile1673=
ENST00000420124.4:c.5019C>A MANE Select	ENSP00000398837.2:p.Ile1673=
ENST00000673918.1:c.4953C>A	ENSP00000501283.1:p.Ile1651=
ENST00000674114.1:c.2341C>A
ENST00000420124.2:c.5019C>A	ENSP00000398837.1:p.Ile1673=
NM_014727.2:c.5019C>A	NP_055542.1:p.Ile1673=
XM_011527561.1:c.4953C>A	XP_011525863.1:p.Ile1651=
XM_011527562.1:c.5019C>A	XP_011525864.1:p.Ile1673=
XM_011527563.1:c.4743C>A	XP_011525865.1:p.Ile1581=
XM_011527561.2:c.4455C>A	XP_011525863.2:p.Ile1485=
XM_011527562.2:c.5019C>A	XP_011525864.1:p.Ile1673=
XM_017027544.1:c.5019C>A	XP_016883033.1:p.Ile1673=
XM_017027545.1:c.4455C>A	XP_016883034.1:p.Ile1485=
XM_017027546.1:c.1983C>A	XP_016883035.1:p.Ile661=
NM_014727.3:c.5019C>A MANE Select	NP_055542.1:p.Ile1673=