Canonical Allele Identifier: CA1010134096
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665733454
gnomAD v3: 1-186673871-TA-T
gnomAD v4: 1-186673871-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673874del , CM000663.2:g.186673874del GRCh38
NC_000001.10:g.186643006del , CM000663.1:g.186643006del GRCh37
NC_000001.9:g.184909629del NCBI36
NG_028206.2:g.11556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*481del MANE Select ENSP00000356438.5:n.*481del
ENST00000680451.1:c.*481del ENSP00000506242.1:n.*481del
ENST00000681605.1:c.*1968del ENSP00000504900.1:n.*1968del
ENST00000367468.9:c.*481del ENSP00000356438.5:n.*481del
ENST00000490885.6:n.2711del
NM_000963.3:c.*481del NP_000954.1:n.*481del
NM_000963.4:c.*481del MANE Select NP_000954.1:n.*481del
Search 100 bp 5'
Search 100 bp 3'