Canonical Allele Identifier: CA405425653

Gene: KMT2B

Linked Data

• dbSNP Id: rs1275015530
• gnomAD v2: 19-36223542-C-T
• gnomAD v4: 19-35732641-C-T
• MyVariant Identifiers: chr19:g.36223542C>T (hg19) ; chr19:g.35732641C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732641C>T , CM000681.2:g.35732641C>T	GRCh38
NC_000019.9:g.36223542C>T , CM000681.1:g.36223542C>T	GRCh37
NC_000019.8:g.40915382C>T	NCBI36
NG_052906.1:g.19623C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.398C>T
ENST00000673918.2:c.6026C>T	ENSP00000501283.1:p.Thr2009Ile
ENST00000674114.2:c.3633C>T	ENSP00000501039.2:n.3633C>T
ENST00000684977.1:c.1310C>T	ENSP00000509384.1:p.Thr437Ile
ENST00000689544.1:n.1245C>T
ENST00000691421.1:c.1313C>T	ENSP00000508674.1:p.Thr438Ile
ENST00000691855.1:c.5634C>T
ENST00000692961.1:c.6092C>T	ENSP00000509289.1:p.Thr2031Ile
ENST00000693677.1:c.704+312C>T	ENSP00000509779.1:n.704+312C>T
ENST00000420124.4:c.6092C>T MANE Select	ENSP00000398837.2:p.Thr2031Ile
ENST00000673918.1:c.6026C>T	ENSP00000501283.1:p.Thr2009Ile
ENST00000674114.1:c.3414C>T
ENST00000420124.2:c.6092C>T	ENSP00000398837.1:p.Thr2031Ile
NM_014727.2:c.6092C>T	NP_055542.1:p.Thr2031Ile
XM_011527561.1:c.6026C>T	XP_011525863.1:p.Thr2009Ile
XM_011527562.1:c.6092C>T	XP_011525864.1:p.Thr2031Ile
XM_011527563.1:c.5816C>T	XP_011525865.1:p.Thr1939Ile
XM_011527561.2:c.5528C>T	XP_011525863.2:p.Thr1843Ile
XM_011527562.2:c.6092C>T	XP_011525864.1:p.Thr2031Ile
XM_017027544.1:c.6092C>T	XP_016883033.1:p.Thr2031Ile
XM_017027545.1:c.5528C>T	XP_016883034.1:p.Thr1843Ile
XM_017027546.1:c.3056C>T	XP_016883035.1:p.Thr1019Ile
NM_014727.3:c.6092C>T MANE Select	NP_055542.1:p.Thr2031Ile