Canonical Allele Identifier: CA199473139

Gene: PTGS1

Linked Data

• dbSNP Id: rs1032090542
• gnomAD v3: 9-122370901-A-T
• gnomAD v4: 9-122370901-A-T
• MyVariant Identifiers: chr9:g.125133180A>T (hg19) ; chr9:g.122370901A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370901A>T , CM000671.2:g.122370901A>T	GRCh38
NC_000009.11:g.125133180A>T , CM000671.1:g.125133180A>T	GRCh37
NC_000009.10:g.124173001A>T	NCBI36
NG_032900.1:g.4952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+59A>T	ENSP00000437709.1:n.-291+59A>T
ENST00000643810.1:c.-321+59A>T	ENSP00000494717.1:n.-321+59A>T
ENST00000540753.5:c.-291+59A>T	ENSP00000437709.1:n.-291+59A>T
NM_001271166.1:c.-321+59A>T	NP_001258095.1:n.-321+59A>T
NM_001271368.1:c.-291+59A>T	NP_001258297.1:n.-291+59A>T
XM_011518875.1:c.-291+59A>T	XP_011517177.1:n.-291+59A>T
XM_011518876.1:c.-4153+59A>T	XP_011517178.1:n.-4153+59A>T
XM_011518875.2:c.-291+59A>T	XP_011517177.1:n.-291+59A>T
XM_011518876.2:c.-4153+59A>T	XP_011517178.1:n.-4153+59A>T
XM_024447614.1:c.-321+59A>T	XP_024303382.1:n.-321+59A>T
XM_024447615.1:c.-321+59A>T	XP_024303383.1:n.-321+59A>T
NM_001271166.2:c.-321+59A>T	NP_001258095.1:n.-321+59A>T
NM_001271368.2:c.-291+59A>T	NP_001258297.1:n.-291+59A>T