Canonical Allele Identifier: CA1141647882
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673759A= , CM000663.2:g.186673759A= GRCh38
NC_000001.10:g.186642891A= , CM000663.1:g.186642891A= GRCh37
NC_000001.9:g.184909514A= NCBI36
NG_028206.2:g.11669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*594T= MANE Select ENSP00000356438.5:n.*594T=
ENST00000680451.1:c.*594T= ENSP00000506242.1:n.*594T=
ENST00000681605.1:c.*2081T= ENSP00000504900.1:n.*2081T=
ENST00000367468.9:c.*594T= ENSP00000356438.5:n.*594T=
ENST00000490885.6:n.2824T=
NM_000963.3:c.*594T= NP_000954.1:n.*594T=
NM_000963.4:c.*594T= MANE Select NP_000954.1:n.*594T=