Canonical Allele Identifier: CA1010134062
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665732376
gnomAD v3: 1-186673811-A-T
gnomAD v4: 1-186673811-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673811A>T , CM000663.2:g.186673811A>T GRCh38
NC_000001.10:g.186642943A>T , CM000663.1:g.186642943A>T GRCh37
NC_000001.9:g.184909566A>T NCBI36
NG_028206.2:g.11617T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*542T>A MANE Select ENSP00000356438.5:n.*542T>A
ENST00000680451.1:c.*542T>A ENSP00000506242.1:n.*542T>A
ENST00000681605.1:c.*2029T>A ENSP00000504900.1:n.*2029T>A
ENST00000367468.9:c.*542T>A ENSP00000356438.5:n.*542T>A
ENST00000490885.6:n.2772T>A
NM_000963.3:c.*542T>A NP_000954.1:n.*542T>A
NM_000963.4:c.*542T>A MANE Select NP_000954.1:n.*542T>A
Search 100 bp 5'
Search 100 bp 3'