Canonical Allele Identifier: CA199473090

Gene: PTGS1

Linked Data

• dbSNP Id: rs76639084
• gnomAD v2: 9-125133094-A-C
• gnomAD v3: 9-122370815-A-C
• gnomAD v4: 9-122370815-A-C
• MyVariant Identifiers: chr9:g.125133094A>C (hg19) ; chr9:g.122370815A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370815A>C , CM000671.2:g.122370815A>C	GRCh38
NC_000009.11:g.125133094A>C , CM000671.1:g.125133094A>C	GRCh37
NC_000009.10:g.124172915A>C	NCBI36
NG_032900.1:g.4866A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-318A>C	ENSP00000437709.1:n.-318A>C
ENST00000643810.1:c.-348A>C	ENSP00000494717.1:n.-348A>C
ENST00000540753.5:c.-318A>C	ENSP00000437709.1:n.-318A>C
NM_001271166.1:c.-348A>C	NP_001258095.1:n.-348A>C
NM_001271368.1:c.-318A>C	NP_001258297.1:n.-318A>C
XM_011518875.1:c.-318A>C	XP_011517177.1:n.-318A>C
XM_011518876.1:c.-4180A>C	XP_011517178.1:n.-4180A>C
XM_011518875.2:c.-318A>C	XP_011517177.1:n.-318A>C
XM_011518876.2:c.-4180A>C	XP_011517178.1:n.-4180A>C
XM_024447614.1:c.-348A>C	XP_024303382.1:n.-348A>C
XM_024447615.1:c.-348A>C	XP_024303383.1:n.-348A>C
NM_001271166.2:c.-348A>C	NP_001258095.1:n.-348A>C
NM_001271368.2:c.-318A>C	NP_001258297.1:n.-318A>C