Canonical Allele Identifier: CA2649581951
Gene: PTGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673875T>C , CM000663.2:g.186673875T>C GRCh38
NC_000001.10:g.186643007T>C , CM000663.1:g.186643007T>C GRCh37
NC_000001.9:g.184909630T>C NCBI36
NG_028206.2:g.11553A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*478A>G MANE Select ENSP00000356438.5:n.*478A>G
ENST00000680451.1:c.*478A>G ENSP00000506242.1:n.*478A>G
ENST00000681605.1:c.*1965A>G ENSP00000504900.1:n.*1965A>G
ENST00000367468.9:c.*478A>G ENSP00000356438.5:n.*478A>G
ENST00000490885.6:n.2708A>G
NM_000963.3:c.*478A>G NP_000954.1:n.*478A>G
NM_000963.4:c.*478A>G MANE Select NP_000954.1:n.*478A>G