Canonical Allele Identifier: CA1010113405
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665865241

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680606C>T , CM000663.2:g.186680606C>T GRCh38
NC_000001.10:g.186649738C>T , CM000663.1:g.186649738C>T GRCh37
NC_000001.9:g.184916361C>T NCBI36
NG_028206.2:g.4822G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+98G>A ENSP00000506242.1:n.-114+98G>A