Canonical Allele Identifier: CA2649583441

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186680593-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680593A>G , CM000663.2:g.186680593A>G	GRCh38
NC_000001.10:g.186649725A>G , CM000663.1:g.186649725A>G	GRCh37
NC_000001.9:g.184916348A>G	NCBI36
NG_028206.2:g.4835T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000680451.1:c.-114+111T>C	ENSP00000506242.1:n.-114+111T>C