Canonical Allele Identifier: CA1213245700
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs919429475

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680512C>A , CM000663.2:g.186680512C>A GRCh38
NC_000001.10:g.186649644C>A , CM000663.1:g.186649644C>A GRCh37
NC_000001.9:g.184916267C>A NCBI36
NG_028206.2:g.4916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-113-109G>T ENSP00000506242.1:n.-113-109G>T