Canonical Allele Identifier: CA34081815
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs918251275

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673912G>A , CM000663.2:g.186673912G>A GRCh38
NC_000001.10:g.186643044G>A , CM000663.1:g.186643044G>A GRCh37
NC_000001.9:g.184909667G>A NCBI36
NG_028206.2:g.11516C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*441C>T MANE Select ENSP00000356438.5:n.*441C>T
ENST00000680451.1:c.*441C>T ENSP00000506242.1:n.*441C>T
ENST00000681605.1:c.*1928C>T ENSP00000504900.1:n.*1928C>T
ENST00000367468.9:c.*441C>T ENSP00000356438.5:n.*441C>T
ENST00000490885.6:n.2671C>T
NM_000963.3:c.*441C>T NP_000954.1:n.*441C>T
NM_000963.4:c.*441C>T MANE Select NP_000954.1:n.*441C>T