Canonical Allele Identifier: CA527766476
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs900370263
gnomAD v2: 1-186649426-A-T
gnomAD v4: 1-186680294-A-T
MyVariant Identifiers: chr1:g.186649426A>T (hg19) chr1:g.186680294A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680294A>T , CM000663.2:g.186680294A>T GRCh38
NC_000001.10:g.186649426A>T , CM000663.1:g.186649426A>T GRCh37
NC_000001.9:g.184916049A>T NCBI36
NG_028206.2:g.5134T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-4T>A MANE Select ENSP00000356438.5:n.-4T>A
ENST00000680451.1:c.-4T>A ENSP00000506242.1:n.-4T>A
ENST00000681605.1:c.-4T>A ENSP00000504900.1:n.-4T>A
ENST00000367468.9:c.-4T>A ENSP00000356438.5:n.-4T>A
ENST00000490885.6:n.130T>A
ENST00000559800.1:n.130T>A
NM_000963.3:c.-4T>A NP_000954.1:n.-4T>A
NM_000963.4:c.-4T>A MANE Select NP_000954.1:n.-4T>A
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