Canonical Allele Identifier: CA1148446238
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673763C= , CM000663.2:g.186673763C= GRCh38
NC_000001.10:g.186642895C= , CM000663.1:g.186642895C= GRCh37
NC_000001.9:g.184909518C= NCBI36
NG_028206.2:g.11665G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*590G= MANE Select ENSP00000356438.5:n.*590G=
ENST00000680451.1:c.*590G= ENSP00000506242.1:n.*590G=
ENST00000681605.1:c.*2077G= ENSP00000504900.1:n.*2077G=
ENST00000367468.9:c.*590G= ENSP00000356438.5:n.*590G=
ENST00000490885.6:n.2820G=
NM_000963.3:c.*590G= NP_000954.1:n.*590G=
NM_000963.4:c.*590G= MANE Select NP_000954.1:n.*590G=