Canonical Allele Identifier: CA2832537996
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680568dup , CM000663.2:g.186680568dup GRCh38
NC_000001.10:g.186649700dup , CM000663.1:g.186649700dup GRCh37
NC_000001.9:g.184916323dup NCBI36
NG_028206.2:g.4864dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-114+140dup ENSP00000506242.1:n.-114+140dup