Canonical Allele Identifier: CA1213245752
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680599T= , CM000663.2:g.186680599T= GRCh38
NC_000001.10:g.186649731T= , CM000663.1:g.186649731T= GRCh37
NC_000001.9:g.184916354T= NCBI36
NG_028206.2:g.4829A=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+105A= ENSP00000506242.1:n.-114+105A=