Canonical Allele Identifier: CA2649581962
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186673917-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673917C>T , CM000663.2:g.186673917C>T GRCh38
NC_000001.10:g.186643049C>T , CM000663.1:g.186643049C>T GRCh37
NC_000001.9:g.184909672C>T NCBI36
NG_028206.2:g.11511G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*436G>A MANE Select ENSP00000356438.5:n.*436G>A
ENST00000680451.1:c.*436G>A ENSP00000506242.1:n.*436G>A
ENST00000681605.1:c.*1923G>A ENSP00000504900.1:n.*1923G>A
ENST00000367468.9:c.*436G>A ENSP00000356438.5:n.*436G>A
ENST00000490885.6:n.2666G>A
NM_000963.3:c.*436G>A NP_000954.1:n.*436G>A
NM_000963.4:c.*436G>A MANE Select NP_000954.1:n.*436G>A
Search 100 bp 5'
Search 100 bp 3'