Canonical Allele Identifier: CA2649583412
Gene: PTGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680558C>A , CM000663.2:g.186680558C>A GRCh38
NC_000001.10:g.186649690C>A , CM000663.1:g.186649690C>A GRCh37
NC_000001.9:g.184916313C>A NCBI36
NG_028206.2:g.4870G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-114+146G>T ENSP00000506242.1:n.-114+146G>T