Canonical Allele Identifier: CA1213245686
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680488C= , CM000663.2:g.186680488C= GRCh38
NC_000001.10:g.186649620C= , CM000663.1:g.186649620C= GRCh37
NC_000001.9:g.184916243C= NCBI36
NG_028206.2:g.4940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-113-85G= ENSP00000506242.1:n.-113-85G=