Canonical Allele Identifier: CA1213245681
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665861449

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680456_186680458dup , CM000663.2:g.186680456_186680458dup GRCh38
NC_000001.10:g.186649588_186649590dup , CM000663.1:g.186649588_186649590dup GRCh37
NC_000001.9:g.184916211_184916213dup NCBI36
NG_028206.2:g.4971_4973dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-113-54_-113-52dup ENSP00000506242.1:n.-113-54_-113-52dup