Canonical Allele Identifier: CA1010113317
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665862220

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680497T>C , CM000663.2:g.186680497T>C GRCh38
NC_000001.10:g.186649629T>C , CM000663.1:g.186649629T>C GRCh37
NC_000001.9:g.184916252T>C NCBI36
NG_028206.2:g.4931A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-94A>G ENSP00000506242.1:n.-113-94A>G