Canonical Allele Identifier: CA2649583337
Gene: PTGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680510A>T , CM000663.2:g.186680510A>T GRCh38
NC_000001.10:g.186649642A>T , CM000663.1:g.186649642A>T GRCh37
NC_000001.9:g.184916265A>T NCBI36
NG_028206.2:g.4918T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-107T>A ENSP00000506242.1:n.-113-107T>A