Canonical Allele Identifier: CA1213245749
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1558252649

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680591T>C , CM000663.2:g.186680591T>C GRCh38
NC_000001.10:g.186649723T>C , CM000663.1:g.186649723T>C GRCh37
NC_000001.9:g.184916346T>C NCBI36
NG_028206.2:g.4837A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+113A>G ENSP00000506242.1:n.-114+113A>G