Canonical Allele Identifier: CA34082458
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1024214523

Genomic Alleles

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

Transcript Alleles

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