Canonical Allele Identifier: CA507308373

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223966C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733065C>T , CM000681.2:g.35733065C>T	GRCh38
NC_000019.9:g.36223966C>T , CM000681.1:g.36223966C>T	GRCh37
NC_000019.8:g.40915806C>T	NCBI36
NG_052906.1:g.20047C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.822C>T
ENST00000673918.2:c.6450C>T	ENSP00000501283.1:p.Val2150=
ENST00000674114.2:c.4057C>T	ENSP00000501039.2:n.4057C>T
ENST00000684977.1:c.1734C>T	ENSP00000509384.1:p.Val578=
ENST00000689544.1:n.1669C>T
ENST00000691421.1:c.1737C>T	ENSP00000508674.1:p.Val579=
ENST00000691855.1:c.6058C>T
ENST00000692961.1:c.6516C>T	ENSP00000509289.1:p.Val2172=
ENST00000693677.1:c.705-532C>T	ENSP00000509779.1:n.705-532C>T
ENST00000420124.4:c.6516C>T MANE Select	ENSP00000398837.2:p.Val2172=
ENST00000673918.1:c.6450C>T	ENSP00000501283.1:p.Val2150=
ENST00000674114.1:c.3838C>T
ENST00000420124.2:c.6516C>T	ENSP00000398837.1:p.Val2172=
NM_014727.2:c.6516C>T	NP_055542.1:p.Val2172=
XM_011527561.1:c.6450C>T	XP_011525863.1:p.Val2150=
XM_011527562.1:c.6516C>T	XP_011525864.1:p.Val2172=
XM_011527563.1:c.6240C>T	XP_011525865.1:p.Val2080=
XM_011527561.2:c.5952C>T	XP_011525863.2:p.Val1984=
XM_011527562.2:c.6516C>T	XP_011525864.1:p.Val2172=
XM_017027544.1:c.6516C>T	XP_016883033.1:p.Val2172=
XM_017027545.1:c.5952C>T	XP_016883034.1:p.Val1984=
XM_017027546.1:c.3480C>T	XP_016883035.1:p.Val1160=
NM_014727.3:c.6516C>T MANE Select	NP_055542.1:p.Val2172=