Canonical Allele Identifier: CA507308099

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223406C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732505C>T , CM000681.2:g.35732505C>T	GRCh38
NC_000019.9:g.36223406C>T , CM000681.1:g.36223406C>T	GRCh37
NC_000019.8:g.40915246C>T	NCBI36
NG_052906.1:g.19487C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.262C>T
ENST00000673918.2:c.5890C>T	ENSP00000501283.1:p.Leu1964=
ENST00000674114.2:c.3497C>T	ENSP00000501039.2:n.3497C>T
ENST00000684977.1:c.1174C>T	ENSP00000509384.1:p.Leu392=
ENST00000689544.1:n.1109C>T
ENST00000691421.1:c.1177C>T	ENSP00000508674.1:p.Leu393=
ENST00000691855.1:c.5498C>T
ENST00000692961.1:c.5956C>T	ENSP00000509289.1:p.Leu1986=
ENST00000693677.1:c.704+176C>T	ENSP00000509779.1:n.704+176C>T
ENST00000420124.4:c.5956C>T MANE Select	ENSP00000398837.2:p.Leu1986=
ENST00000673918.1:c.5890C>T	ENSP00000501283.1:p.Leu1964=
ENST00000674114.1:c.3278C>T
ENST00000420124.2:c.5956C>T	ENSP00000398837.1:p.Leu1986=
NM_014727.2:c.5956C>T	NP_055542.1:p.Leu1986=
XM_011527561.1:c.5890C>T	XP_011525863.1:p.Leu1964=
XM_011527562.1:c.5956C>T	XP_011525864.1:p.Leu1986=
XM_011527563.1:c.5680C>T	XP_011525865.1:p.Leu1894=
XM_011527561.2:c.5392C>T	XP_011525863.2:p.Leu1798=
XM_011527562.2:c.5956C>T	XP_011525864.1:p.Leu1986=
XM_017027544.1:c.5956C>T	XP_016883033.1:p.Leu1986=
XM_017027545.1:c.5392C>T	XP_016883034.1:p.Leu1798=
XM_017027546.1:c.2920C>T	XP_016883035.1:p.Leu974=
NM_014727.3:c.5956C>T MANE Select	NP_055542.1:p.Leu1986=