Canonical Allele Identifier: CA2746992947
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673826G>T , CM000663.2:g.186673826G>T GRCh38
NC_000001.10:g.186642958G>T , CM000663.1:g.186642958G>T GRCh37
NC_000001.9:g.184909581G>T NCBI36
NG_028206.2:g.11602C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*527C>A MANE Select ENSP00000356438.5:n.*527C>A
ENST00000680451.1:c.*527C>A ENSP00000506242.1:n.*527C>A
ENST00000681605.1:c.*2014C>A ENSP00000504900.1:n.*2014C>A
ENST00000367468.9:c.*527C>A ENSP00000356438.5:n.*527C>A
ENST00000490885.6:n.2757C>A
NM_000963.3:c.*527C>A NP_000954.1:n.*527C>A
NM_000963.4:c.*527C>A MANE Select NP_000954.1:n.*527C>A
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