Canonical Allele Identifier: CA1213245747
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680590A= , CM000663.2:g.186680590A= GRCh38
NC_000001.10:g.186649722A= , CM000663.1:g.186649722A= GRCh37
NC_000001.9:g.184916345A= NCBI36
NG_028206.2:g.4838T=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+114T= ENSP00000506242.1:n.-114+114T=