Canonical Allele Identifier: CA1213245748
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680591T= , CM000663.2:g.186680591T= GRCh38
NC_000001.10:g.186649723T= , CM000663.1:g.186649723T= GRCh37
NC_000001.9:g.184916346T= NCBI36
NG_028206.2:g.4837A=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+113A= ENSP00000506242.1:n.-114+113A=