Canonical Allele Identifier: CA507072585

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220927C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730026C>G , CM000681.2:g.35730026C>G	GRCh38
NC_000019.9:g.36220927C>G , CM000681.1:g.36220927C>G	GRCh37
NC_000019.8:g.40912767C>G	NCBI36
NG_052906.1:g.17008C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4911C>G	ENSP00000501283.1:p.Leu1637=
ENST00000674114.2:c.2518C>G	ENSP00000501039.2:n.2518C>G
ENST00000684977.1:c.195C>G	ENSP00000509384.1:p.Leu65=
ENST00000685168.1:c.403C>G
ENST00000689544.1:n.130C>G
ENST00000691421.1:c.198C>G	ENSP00000508674.1:p.Leu66=
ENST00000691855.1:c.4519C>G
ENST00000692961.1:c.4977C>G	ENSP00000509289.1:p.Leu1659=
ENST00000420124.4:c.4977C>G MANE Select	ENSP00000398837.2:p.Leu1659=
ENST00000673918.1:c.4911C>G	ENSP00000501283.1:p.Leu1637=
ENST00000674114.1:c.2299C>G
ENST00000420124.2:c.4977C>G	ENSP00000398837.1:p.Leu1659=
NM_014727.2:c.4977C>G	NP_055542.1:p.Leu1659=
XM_011527561.1:c.4911C>G	XP_011525863.1:p.Leu1637=
XM_011527562.1:c.4977C>G	XP_011525864.1:p.Leu1659=
XM_011527563.1:c.4701C>G	XP_011525865.1:p.Leu1567=
XM_011527561.2:c.4413C>G	XP_011525863.2:p.Leu1471=
XM_011527562.2:c.4977C>G	XP_011525864.1:p.Leu1659=
XM_017027544.1:c.4977C>G	XP_016883033.1:p.Leu1659=
XM_017027545.1:c.4413C>G	XP_016883034.1:p.Leu1471=
XM_017027546.1:c.1941C>G	XP_016883035.1:p.Leu647=
NM_014727.3:c.4977C>G MANE Select	NP_055542.1:p.Leu1659=