Canonical Allele Identifier: CA422374358
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs2102008676
MyVariant Identifiers: chr1:g.186650006C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680874C>T , CM000663.2:g.186680874C>T GRCh38
NC_000001.10:g.186650006C>T , CM000663.1:g.186650006C>T GRCh37
NC_000001.9:g.184916629C>T NCBI36
NG_028206.2:g.4554G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-284G>A (PTGS2) ENSP00000506242.1:n.-284G>A
NR_125801.1:n.221C>T (PACERR)
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