Canonical Allele Identifier: CA528080528
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs567818121
gnomAD v2: 1-186650008-C-CCCG
gnomAD v3: 1-186680876-C-CCCG
gnomAD v4: 1-186680876-C-CCCG
MyVariant Identifiers: chr1:g.186650011_186650012insCCG (hg19) chr1:g.186650008_186650009insCCG (hg19) chr1:g.186680879_186680880insCCG (hg38) chr1:g.186680876_186680877insCCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680889_186680891dup , CM000663.2:g.186680889_186680891dup GRCh38
NC_000001.10:g.186650021_186650023dup , CM000663.1:g.186650021_186650023dup GRCh37
NC_000001.9:g.184916644_184916646dup NCBI36
NG_028206.2:g.4549_4551dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-289_-287dup (PTGS2) ENSP00000506242.1:n.-289_-287dup
NR_125801.1:n.236_238dup (PACERR)
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