Canonical Allele Identifier: CA2691550003
Gene: PTGS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122370799C>A , CM000671.2:g.122370799C>A GRCh38
NC_000009.11:g.125133078C>A , CM000671.1:g.125133078C>A GRCh37
NC_000009.10:g.124172899C>A NCBI36
NG_032900.1:g.4850C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000540753.6:c.-334C>A ENSP00000437709.1:n.-334C>A
ENST00000643810.1:c.-364C>A ENSP00000494717.1:n.-364C>A
ENST00000540753.5:c.-334C>A ENSP00000437709.1:n.-334C>A
NM_001271166.1:c.-364C>A NP_001258095.1:n.-364C>A
NM_001271368.1:c.-334C>A NP_001258297.1:n.-334C>A
XM_011518875.1:c.-334C>A XP_011517177.1:n.-334C>A
XM_011518876.1:c.-4196C>A XP_011517178.1:n.-4196C>A
XM_011518875.2:c.-334C>A XP_011517177.1:n.-334C>A
XM_011518876.2:c.-4196C>A XP_011517178.1:n.-4196C>A
XM_024447614.1:c.-364C>A XP_024303382.1:n.-364C>A
XM_024447615.1:c.-364C>A XP_024303383.1:n.-364C>A
NM_001271166.2:c.-364C>A NP_001258095.1:n.-364C>A
NM_001271368.2:c.-334C>A NP_001258297.1:n.-334C>A