Canonical Allele Identifier: CA2649583147
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680310-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680310C>T , CM000663.2:g.186680310C>T GRCh38
NC_000001.10:g.186649442C>T , CM000663.1:g.186649442C>T GRCh37
NC_000001.9:g.184916065C>T NCBI36
NG_028206.2:g.5118G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-20G>A MANE Select ENSP00000356438.5:n.-20G>A
ENST00000680451.1:c.-20G>A ENSP00000506242.1:n.-20G>A
ENST00000681605.1:c.-20G>A ENSP00000504900.1:n.-20G>A
ENST00000367468.9:c.-20G>A ENSP00000356438.5:n.-20G>A
ENST00000490885.6:n.114G>A
ENST00000559800.1:n.114G>A
NM_000963.3:c.-20G>A NP_000954.1:n.-20G>A
NM_000963.4:c.-20G>A MANE Select NP_000954.1:n.-20G>A
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