Canonical Allele Identifier: CA2691550016

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370814-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370814T>C , CM000671.2:g.122370814T>C	GRCh38
NC_000009.11:g.125133093T>C , CM000671.1:g.125133093T>C	GRCh37
NC_000009.10:g.124172914T>C	NCBI36
NG_032900.1:g.4865T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-319T>C	ENSP00000437709.1:n.-319T>C
ENST00000643810.1:c.-349T>C	ENSP00000494717.1:n.-349T>C
ENST00000540753.5:c.-319T>C	ENSP00000437709.1:n.-319T>C
NM_001271166.1:c.-349T>C	NP_001258095.1:n.-349T>C
NM_001271368.1:c.-319T>C	NP_001258297.1:n.-319T>C
XM_011518875.1:c.-319T>C	XP_011517177.1:n.-319T>C
XM_011518876.1:c.-4181T>C	XP_011517178.1:n.-4181T>C
XM_011518875.2:c.-319T>C	XP_011517177.1:n.-319T>C
XM_011518876.2:c.-4181T>C	XP_011517178.1:n.-4181T>C
XM_024447614.1:c.-349T>C	XP_024303382.1:n.-349T>C
XM_024447615.1:c.-349T>C	XP_024303383.1:n.-349T>C
NM_001271166.2:c.-349T>C	NP_001258095.1:n.-349T>C
NM_001271368.2:c.-319T>C	NP_001258297.1:n.-319T>C