Canonical Allele Identifier: CA859722636

Gene: PTGS1

Linked Data

• dbSNP Id: rs1233480540
• gnomAD v3: 9-122370765-C-T
• gnomAD v4: 9-122370765-C-T
• MyVariant Identifiers: chr9:g.125133044C>T (hg19) ; chr9:g.122370765C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370765C>T , CM000671.2:g.122370765C>T	GRCh38
NC_000009.11:g.125133044C>T , CM000671.1:g.125133044C>T	GRCh37
NC_000009.10:g.124172865C>T	NCBI36
NG_032900.1:g.4816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-368C>T	ENSP00000437709.1:n.-368C>T
ENST00000643810.1:c.-398C>T	ENSP00000494717.1:n.-398C>T
ENST00000540753.5:c.-368C>T	ENSP00000437709.1:n.-368C>T
NM_001271166.1:c.-398C>T	NP_001258095.1:n.-398C>T
NM_001271368.1:c.-368C>T	NP_001258297.1:n.-368C>T
XM_011518875.1:c.-368C>T	XP_011517177.1:n.-368C>T
XM_011518876.1:c.-4230C>T	XP_011517178.1:n.-4230C>T
XM_011518875.2:c.-368C>T	XP_011517177.1:n.-368C>T
XM_011518876.2:c.-4230C>T	XP_011517178.1:n.-4230C>T
XM_024447614.1:c.-398C>T	XP_024303382.1:n.-398C>T
XM_024447615.1:c.-398C>T	XP_024303383.1:n.-398C>T
NM_001271166.2:c.-398C>T	NP_001258095.1:n.-398C>T
NM_001271368.2:c.-368C>T	NP_001258297.1:n.-368C>T