Canonical Allele Identifier: CA507072616

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220942C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730041C>T , CM000681.2:g.35730041C>T	GRCh38
NC_000019.9:g.36220942C>T , CM000681.1:g.36220942C>T	GRCh37
NC_000019.8:g.40912782C>T	NCBI36
NG_052906.1:g.17023C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000673918.2:c.4926C>T	ENSP00000501283.1:p.Phe1642=
ENST00000674114.2:c.2533C>T	ENSP00000501039.2:n.2533C>T
ENST00000684977.1:c.210C>T	ENSP00000509384.1:p.Phe70=
ENST00000685168.1:c.418C>T
ENST00000689544.1:n.145C>T
ENST00000691421.1:c.213C>T	ENSP00000508674.1:p.Phe71=
ENST00000691855.1:c.4534C>T
ENST00000692961.1:c.4992C>T	ENSP00000509289.1:p.Phe1664=
ENST00000420124.4:c.4992C>T MANE Select	ENSP00000398837.2:p.Phe1664=
ENST00000673918.1:c.4926C>T	ENSP00000501283.1:p.Phe1642=
ENST00000674114.1:c.2314C>T
ENST00000420124.2:c.4992C>T	ENSP00000398837.1:p.Phe1664=
NM_014727.2:c.4992C>T	NP_055542.1:p.Phe1664=
XM_011527561.1:c.4926C>T	XP_011525863.1:p.Phe1642=
XM_011527562.1:c.4992C>T	XP_011525864.1:p.Phe1664=
XM_011527563.1:c.4716C>T	XP_011525865.1:p.Phe1572=
XM_011527561.2:c.4428C>T	XP_011525863.2:p.Phe1476=
XM_011527562.2:c.4992C>T	XP_011525864.1:p.Phe1664=
XM_017027544.1:c.4992C>T	XP_016883033.1:p.Phe1664=
XM_017027545.1:c.4428C>T	XP_016883034.1:p.Phe1476=
XM_017027546.1:c.1956C>T	XP_016883035.1:p.Phe652=
NM_014727.3:c.4992C>T MANE Select	NP_055542.1:p.Phe1664=