Canonical Allele Identifier: CA507308496

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223570T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732669T>G , CM000681.2:g.35732669T>G	GRCh38
NC_000019.9:g.36223570T>G , CM000681.1:g.36223570T>G	GRCh37
NC_000019.8:g.40915410T>G	NCBI36
NG_052906.1:g.19651T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.426T>G
ENST00000673918.2:c.6054T>G	ENSP00000501283.1:p.Thr2018=
ENST00000674114.2:c.3661T>G	ENSP00000501039.2:n.3661T>G
ENST00000684977.1:c.1338T>G	ENSP00000509384.1:p.Thr446=
ENST00000689544.1:n.1273T>G
ENST00000691421.1:c.1341T>G	ENSP00000508674.1:p.Thr447=
ENST00000691855.1:c.5662T>G
ENST00000692961.1:c.6120T>G	ENSP00000509289.1:p.Thr2040=
ENST00000693677.1:c.704+340T>G	ENSP00000509779.1:n.704+340T>G
ENST00000420124.4:c.6120T>G MANE Select	ENSP00000398837.2:p.Thr2040=
ENST00000673918.1:c.6054T>G	ENSP00000501283.1:p.Thr2018=
ENST00000674114.1:c.3442T>G
ENST00000420124.2:c.6120T>G	ENSP00000398837.1:p.Thr2040=
NM_014727.2:c.6120T>G	NP_055542.1:p.Thr2040=
XM_011527561.1:c.6054T>G	XP_011525863.1:p.Thr2018=
XM_011527562.1:c.6120T>G	XP_011525864.1:p.Thr2040=
XM_011527563.1:c.5844T>G	XP_011525865.1:p.Thr1948=
XM_011527561.2:c.5556T>G	XP_011525863.2:p.Thr1852=
XM_011527562.2:c.6120T>G	XP_011525864.1:p.Thr2040=
XM_017027544.1:c.6120T>G	XP_016883033.1:p.Thr2040=
XM_017027545.1:c.5556T>G	XP_016883034.1:p.Thr1852=
XM_017027546.1:c.3084T>G	XP_016883035.1:p.Thr1028=
NM_014727.3:c.6120T>G MANE Select	NP_055542.1:p.Thr2040=