Canonical Allele Identifier: CA1213245751
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680594G= , CM000663.2:g.186680594G= GRCh38
NC_000001.10:g.186649726G= , CM000663.1:g.186649726G= GRCh37
NC_000001.9:g.184916349G= NCBI36
NG_028206.2:g.4834C=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+110C= ENSP00000506242.1:n.-114+110C=