Canonical Allele Identifier: CA2546578259
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680607C>G , CM000663.2:g.186680607C>G GRCh38
NC_000001.10:g.186649739C>G , CM000663.1:g.186649739C>G GRCh37
NC_000001.9:g.184916362C>G NCBI36
NG_028206.2:g.4821G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+97G>C ENSP00000506242.1:n.-114+97G>C