Canonical Allele Identifier: CA199474263

Gene: PTGS1

Linked Data

• dbSNP Id: rs992056124
• gnomAD v3: 9-122373275-G-A
• gnomAD v4: 9-122373275-G-A
• MyVariant Identifiers: chr9:g.125135554G>A (hg19) ; chr9:g.122373275G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122373275G>A , CM000671.2:g.122373275G>A	GRCh38
NC_000009.11:g.125135554G>A , CM000671.1:g.125135554G>A	GRCh37
NC_000009.10:g.124175375G>A	NCBI36
NG_032900.1:g.7326G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.94+2003G>A MANE Select	ENSP00000354612.2:n.94+2003G>A
ENST00000426608.6:c.94+2003G>A	ENSP00000411606.2:n.94+2003G>A
ENST00000540753.6:c.19+1441G>A	ENSP00000437709.1:n.19+1441G>A
ENST00000619306.5:c.94+2003G>A	ENSP00000483540.2:n.94+2003G>A
ENST00000643576.1:n.188+2003G>A
ENST00000643810.1:c.-234+2003G>A	ENSP00000494717.1:n.-234+2003G>A
ENST00000645132.1:n.261+2003G>A
ENST00000647067.1:c.94+2003G>A	ENSP00000495728.1:n.94+2003G>A
ENST00000223423.8:c.94+2003G>A	ENSP00000223423.4:n.94+2003G>A
ENST00000362012.6:c.94+2003G>A	ENSP00000354612.2:n.94+2003G>A
ENST00000426608.5:c.85+2003G>A	ENSP00000411606.1:n.85+2003G>A
ENST00000540753.5:c.19+1441G>A	ENSP00000437709.1:n.19+1441G>A
ENST00000614910.4:c.94+2003G>A	ENSP00000484800.1:n.94+2003G>A
ENST00000619306.4:c.187+2003G>A	ENSP00000483540.1:n.187+2003G>A
NM_000962.3:c.94+2003G>A	NP_000953.2:n.94+2003G>A
NM_001271164.1:c.94+2003G>A	NP_001258093.1:n.94+2003G>A
NM_001271166.1:c.-234+2003G>A	NP_001258095.1:n.-234+2003G>A
NM_001271367.1:c.-205+2003G>A	NP_001258296.1:n.-205+2003G>A
NM_001271368.1:c.19+1441G>A	NP_001258297.1:n.19+1441G>A
NM_080591.2:c.94+2003G>A	NP_542158.1:n.94+2003G>A
XM_005252105.2:c.19+1441G>A	XP_005252162.1:n.19+1441G>A
XM_011518875.1:c.19+1441G>A	XP_011517177.1:n.19+1441G>A
XM_011518876.1:c.-2403G>A	XP_011517178.1:n.-2403G>A
XM_005252105.3:c.19+1441G>A	XP_005252162.1:n.19+1441G>A
XM_011518875.2:c.19+1441G>A	XP_011517177.1:n.19+1441G>A
XM_011518876.2:c.-2403G>A	XP_011517178.1:n.-2403G>A
XM_024447614.1:c.-234+2003G>A	XP_024303382.1:n.-234+2003G>A
XM_024447615.1:c.-234+2003G>A	XP_024303383.1:n.-234+2003G>A
NM_000962.4:c.94+2003G>A MANE Select	NP_000953.2:n.94+2003G>A
NM_001271164.2:c.94+2003G>A	NP_001258093.1:n.94+2003G>A
NM_001271166.2:c.-234+2003G>A	NP_001258095.1:n.-234+2003G>A
NM_001271367.2:c.-205+2003G>A	NP_001258296.1:n.-205+2003G>A
NM_001271368.2:c.19+1441G>A	NP_001258297.1:n.19+1441G>A
NM_080591.3:c.94+2003G>A	NP_542158.1:n.94+2003G>A