Canonical Allele Identifier: CA34082478
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs993921259
gnomAD v3: 1-186680732-C-G
gnomAD v4: 1-186680732-C-G
MyVariant Identifiers: chr1:g.186649864C>G (hg19) chr1:g.186680732C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680732C>G , CM000663.2:g.186680732C>G GRCh38
NC_000001.10:g.186649864C>G , CM000663.1:g.186649864C>G GRCh37
NC_000001.9:g.184916487C>G NCBI36
NG_028206.2:g.4696G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-142G>C (PTGS2) ENSP00000506242.1:n.-142G>C
NR_125801.1:n.79C>G (PACERR)
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