Canonical Allele Identifier: CA199473102

Gene: PTGS1

Linked Data

• dbSNP Id: rs576028663
• gnomAD v2: 9-125133108-C-G
• gnomAD v3: 9-122370829-C-G
• gnomAD v4: 9-122370829-C-G
• MyVariant Identifiers: chr9:g.125133108C>G (hg19) ; chr9:g.122370829C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370829C>G , CM000671.2:g.122370829C>G	GRCh38
NC_000009.11:g.125133108C>G , CM000671.1:g.125133108C>G	GRCh37
NC_000009.10:g.124172929C>G	NCBI36
NG_032900.1:g.4880C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-304C>G	ENSP00000437709.1:n.-304C>G
ENST00000643810.1:c.-334C>G	ENSP00000494717.1:n.-334C>G
ENST00000540753.5:c.-304C>G	ENSP00000437709.1:n.-304C>G
NM_001271166.1:c.-334C>G	NP_001258095.1:n.-334C>G
NM_001271368.1:c.-304C>G	NP_001258297.1:n.-304C>G
XM_011518875.1:c.-304C>G	XP_011517177.1:n.-304C>G
XM_011518876.1:c.-4166C>G	XP_011517178.1:n.-4166C>G
XM_011518875.2:c.-304C>G	XP_011517177.1:n.-304C>G
XM_011518876.2:c.-4166C>G	XP_011517178.1:n.-4166C>G
XM_024447614.1:c.-334C>G	XP_024303382.1:n.-334C>G
XM_024447615.1:c.-334C>G	XP_024303383.1:n.-334C>G
NM_001271166.2:c.-334C>G	NP_001258095.1:n.-334C>G
NM_001271368.2:c.-304C>G	NP_001258297.1:n.-304C>G