Canonical Allele Identifier: CA859722663

Gene: PTGS1

Linked Data

• dbSNP Id: rs1288717257
• gnomAD v3: 9-122370793-T-C
• gnomAD v4: 9-122370793-T-C
• MyVariant Identifiers: chr9:g.125133072T>C (hg19) ; chr9:g.122370793T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370793T>C , CM000671.2:g.122370793T>C	GRCh38
NC_000009.11:g.125133072T>C , CM000671.1:g.125133072T>C	GRCh37
NC_000009.10:g.124172893T>C	NCBI36
NG_032900.1:g.4844T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-340T>C	ENSP00000437709.1:n.-340T>C
ENST00000643810.1:c.-370T>C	ENSP00000494717.1:n.-370T>C
ENST00000540753.5:c.-340T>C	ENSP00000437709.1:n.-340T>C
NM_001271166.1:c.-370T>C	NP_001258095.1:n.-370T>C
NM_001271368.1:c.-340T>C	NP_001258297.1:n.-340T>C
XM_011518875.1:c.-340T>C	XP_011517177.1:n.-340T>C
XM_011518876.1:c.-4202T>C	XP_011517178.1:n.-4202T>C
XM_011518875.2:c.-340T>C	XP_011517177.1:n.-340T>C
XM_011518876.2:c.-4202T>C	XP_011517178.1:n.-4202T>C
XM_024447614.1:c.-370T>C	XP_024303382.1:n.-370T>C
XM_024447615.1:c.-370T>C	XP_024303383.1:n.-370T>C
NM_001271166.2:c.-370T>C	NP_001258095.1:n.-370T>C
NM_001271368.2:c.-340T>C	NP_001258297.1:n.-340T>C