Canonical Allele Identifier: CA2746992949
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673909T>G , CM000663.2:g.186673909T>G GRCh38
NC_000001.10:g.186643041T>G , CM000663.1:g.186643041T>G GRCh37
NC_000001.9:g.184909664T>G NCBI36
NG_028206.2:g.11519A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*444A>C MANE Select ENSP00000356438.5:n.*444A>C
ENST00000680451.1:c.*444A>C ENSP00000506242.1:n.*444A>C
ENST00000681605.1:c.*1931A>C ENSP00000504900.1:n.*1931A>C
ENST00000367468.9:c.*444A>C ENSP00000356438.5:n.*444A>C
ENST00000490885.6:n.2674A>C
NM_000963.3:c.*444A>C NP_000954.1:n.*444A>C
NM_000963.4:c.*444A>C MANE Select NP_000954.1:n.*444A>C
Search 100 bp 5'
Search 100 bp 3'