Canonical Allele Identifier: CA859722665

Gene: PTGS1

Linked Data

• dbSNP Id: rs1374918703
• gnomAD v4: 9-122370803-A-G
• MyVariant Identifiers: chr9:g.125133082A>G (hg19) ; chr9:g.122370803A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370803A>G , CM000671.2:g.122370803A>G	GRCh38
NC_000009.11:g.125133082A>G , CM000671.1:g.125133082A>G	GRCh37
NC_000009.10:g.124172903A>G	NCBI36
NG_032900.1:g.4854A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-330A>G	ENSP00000437709.1:n.-330A>G
ENST00000643810.1:c.-360A>G	ENSP00000494717.1:n.-360A>G
ENST00000540753.5:c.-330A>G	ENSP00000437709.1:n.-330A>G
NM_001271166.1:c.-360A>G	NP_001258095.1:n.-360A>G
NM_001271368.1:c.-330A>G	NP_001258297.1:n.-330A>G
XM_011518875.1:c.-330A>G	XP_011517177.1:n.-330A>G
XM_011518876.1:c.-4192A>G	XP_011517178.1:n.-4192A>G
XM_011518875.2:c.-330A>G	XP_011517177.1:n.-330A>G
XM_011518876.2:c.-4192A>G	XP_011517178.1:n.-4192A>G
XM_024447614.1:c.-360A>G	XP_024303382.1:n.-360A>G
XM_024447615.1:c.-360A>G	XP_024303383.1:n.-360A>G
NM_001271166.2:c.-360A>G	NP_001258095.1:n.-360A>G
NM_001271368.2:c.-330A>G	NP_001258297.1:n.-330A>G