Canonical Allele Identifier: CA1213245690
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680499C= , CM000663.2:g.186680499C= GRCh38
NC_000001.10:g.186649631C= , CM000663.1:g.186649631C= GRCh37
NC_000001.9:g.184916254C= NCBI36
NG_028206.2:g.4929G=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-96G= ENSP00000506242.1:n.-113-96G=