Canonical Allele Identifier: CA34082500
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1020020936
MyVariant Identifiers: chr1:g.186650002C>G (hg19) chr1:g.186680870C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680870C>G , CM000663.2:g.186680870C>G GRCh38
NC_000001.10:g.186650002C>G , CM000663.1:g.186650002C>G GRCh37
NC_000001.9:g.184916625C>G NCBI36
NG_028206.2:g.4558G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-280G>C (PTGS2) ENSP00000506242.1:n.-280G>C
NR_125801.1:n.217C>G (PACERR)
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