Canonical Allele Identifier: CA2649583318

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186680495-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680495T>G , CM000663.2:g.186680495T>G	GRCh38
NC_000001.10:g.186649627T>G , CM000663.1:g.186649627T>G	GRCh37
NC_000001.9:g.184916250T>G	NCBI36
NG_028206.2:g.4933A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000680451.1:c.-113-92A>C	ENSP00000506242.1:n.-113-92A>C