Canonical Allele Identifier: CA422374470
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1665870410
MyVariant Identifiers: chr1:g.186650044A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680912A>G , CM000663.2:g.186680912A>G GRCh38
NC_000001.10:g.186650044A>G , CM000663.1:g.186650044A>G GRCh37
NC_000001.9:g.184916667A>G NCBI36
NG_028206.2:g.4516T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-322T>C (PTGS2) ENSP00000506242.1:n.-322T>C
NR_125801.1:n.259A>G (PACERR)
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