Canonical Allele Identifier: CA1213243948
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673790C= , CM000663.2:g.186673790C= GRCh38
NC_000001.10:g.186642922C= , CM000663.1:g.186642922C= GRCh37
NC_000001.9:g.184909545C= NCBI36
NG_028206.2:g.11638G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*563G= MANE Select ENSP00000356438.5:n.*563G=
ENST00000680451.1:c.*563G= ENSP00000506242.1:n.*563G=
ENST00000681605.1:c.*2050G= ENSP00000504900.1:n.*2050G=
ENST00000367468.9:c.*563G= ENSP00000356438.5:n.*563G=
ENST00000490885.6:n.2793G=
NM_000963.3:c.*563G= NP_000954.1:n.*563G=
NM_000963.4:c.*563G= MANE Select NP_000954.1:n.*563G=