Canonical Allele Identifier: CA528080517
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1341479697
gnomAD v2: 1-186649631-C-A
gnomAD v3: 1-186680499-C-A
gnomAD v4: 1-186680499-C-A
MyVariant Identifiers: chr1:g.186649631C>A (hg19) chr1:g.186680499C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680499C>A , CM000663.2:g.186680499C>A GRCh38
NC_000001.10:g.186649631C>A , CM000663.1:g.186649631C>A GRCh37
NC_000001.9:g.184916254C>A NCBI36
NG_028206.2:g.4929G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-96G>T ENSP00000506242.1:n.-113-96G>T
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