Canonical Allele Identifier: CA528080518
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs970431868
gnomAD v2: 1-186649639-C-G
gnomAD v3: 1-186680507-C-G
gnomAD v4: 1-186680507-C-G
MyVariant Identifiers: chr1:g.186649639C>G (hg19) chr1:g.186680507C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680507C>G , CM000663.2:g.186680507C>G GRCh38
NC_000001.10:g.186649639C>G , CM000663.1:g.186649639C>G GRCh37
NC_000001.9:g.184916262C>G NCBI36
NG_028206.2:g.4921G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-104G>C ENSP00000506242.1:n.-113-104G>C
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