Canonical Allele Identifier: CA34082477
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs578161356
gnomAD v3: 1-186680725-T-C
gnomAD v4: 1-186680725-T-C
MyVariant Identifiers: chr1:g.186649857T>C (hg19) chr1:g.186680725T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680725T>C , CM000663.2:g.186680725T>C GRCh38
NC_000001.10:g.186649857T>C , CM000663.1:g.186649857T>C GRCh37
NC_000001.9:g.184916480T>C NCBI36
NG_028206.2:g.4703A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-135A>G (PTGS2) ENSP00000506242.1:n.-135A>G
NR_125801.1:n.72T>C (PACERR)
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Search 100 bp 3'