Canonical Allele Identifier: CA1143486098
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673846A= , CM000663.2:g.186673846A= GRCh38
NC_000001.10:g.186642978A= , CM000663.1:g.186642978A= GRCh37
NC_000001.9:g.184909601A= NCBI36
NG_028206.2:g.11582T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*507T= MANE Select ENSP00000356438.5:n.*507T=
ENST00000680451.1:c.*507T= ENSP00000506242.1:n.*507T=
ENST00000681605.1:c.*1994T= ENSP00000504900.1:n.*1994T=
ENST00000367468.9:c.*507T= ENSP00000356438.5:n.*507T=
ENST00000490885.6:n.2737T=
NM_000963.3:c.*507T= NP_000954.1:n.*507T=
NM_000963.4:c.*507T= MANE Select NP_000954.1:n.*507T=