Canonical Allele Identifier: CA15602209
Gene: PTGES2 HGNC NCBI

Linked Data

dbSNP Id: rs884115
gnomAD v2: 9-130887856-C-T
gnomAD v3: 9-128125577-C-T
gnomAD v4: 9-128125577-C-T
MyVariant Identifiers: chr9:g.130887856C>T (hg19) chr9:g.128125577C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128125577C>T , CM000671.2:g.128125577C>T GRCh38
NC_000009.11:g.130887856C>T , CM000671.1:g.130887856C>T GRCh37
NC_000009.10:g.129927677C>T NCBI36
NG_012488.1:g.7619G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000338961.11:c.280-136G>A MANE Select ENSP00000345341.6:n.280-136G>A
ENST00000474124.6:c.280-136G>A ENSP00000503197.1:n.280-136G>A
ENST00000476655.6:n.284-136G>A
ENST00000483625.6:n.298-136G>A
ENST00000493205.6:n.1600G>A
ENST00000497109.6:n.295-136G>A
ENST00000676562.1:c.280-39G>A ENSP00000504019.1:n.280-39G>A
ENST00000677651.1:c.280-136G>A ENSP00000502881.1:n.280-136G>A
ENST00000677691.1:c.-294-136G>A ENSP00000503821.1:n.-294-136G>A
ENST00000677980.1:c.*327-136G>A ENSP00000503843.1:n.*327-136G>A
ENST00000678174.1:c.280-136G>A ENSP00000504703.1:n.280-136G>A
ENST00000678916.1:c.280-136G>A ENSP00000504746.1:n.280-136G>A
ENST00000679345.1:c.280-136G>A ENSP00000502870.1:n.280-136G>A
ENST00000277462.9:c.-387-136G>A ENSP00000277462.5:n.-387-136G>A
ENST00000338961.10:c.280-136G>A ENSP00000345341.6:n.280-136G>A
ENST00000449878.1:c.280-241G>A ENSP00000411378.1:n.280-241G>A
ENST00000474124.5:n.238-136G>A
ENST00000476748.5:n.149-136G>A
ENST00000483625.5:n.272-136G>A
ENST00000485237.1:n.61-136G>A
ENST00000485510.5:n.274-136G>A
ENST00000487063.5:n.93-136G>A
ENST00000496594.5:n.280-136G>A
ENST00000497109.5:n.172-136G>A
ENST00000617202.4:c.-198-136G>A ENSP00000482913.1:n.-198-136G>A
NM_001256335.1:c.-198-136G>A NP_001243264.1:n.-198-136G>A
NM_025072.6:c.280-136G>A NP_079348.1:n.280-136G>A
NM_198938.2:c.-387-136G>A NP_945176.1:n.-387-136G>A
XM_005252239.1:c.-387-136G>A XP_005252296.1:n.-387-136G>A
XM_011519050.1:c.-294-136G>A XP_011517352.1:n.-294-136G>A
XM_011519051.1:c.-387-136G>A XP_011517353.1:n.-387-136G>A
XM_005252239.2:c.-387-136G>A XP_005252296.1:n.-387-136G>A
XM_011519051.3:c.-387-136G>A XP_011517353.1:n.-387-136G>A
XM_024447688.1:c.-294-136G>A XP_024303456.1:n.-294-136G>A
XR_001746383.2:n.519-136G>A
NM_025072.7:c.280-136G>A MANE Select NP_079348.1:n.280-136G>A
NM_001256335.2:c.-198-136G>A NP_001243264.1:n.-198-136G>A
NM_198938.3:c.-387-136G>A NP_945176.1:n.-387-136G>A
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