Canonical Allele Identifier: CA1213243938
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673767C= , CM000663.2:g.186673767C= GRCh38
NC_000001.10:g.186642899C= , CM000663.1:g.186642899C= GRCh37
NC_000001.9:g.184909522C= NCBI36
NG_028206.2:g.11661G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*586G= MANE Select ENSP00000356438.5:n.*586G=
ENST00000680451.1:c.*586G= ENSP00000506242.1:n.*586G=
ENST00000681605.1:c.*2073G= ENSP00000504900.1:n.*2073G=
ENST00000367468.9:c.*586G= ENSP00000356438.5:n.*586G=
ENST00000490885.6:n.2816G=
NM_000963.3:c.*586G= NP_000954.1:n.*586G=
NM_000963.4:c.*586G= MANE Select NP_000954.1:n.*586G=