Canonical Allele Identifier: CA1213245760
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665865433

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680610G>A , CM000663.2:g.186680610G>A GRCh38
NC_000001.10:g.186649742G>A , CM000663.1:g.186649742G>A GRCh37
NC_000001.9:g.184916365G>A NCBI36
NG_028206.2:g.4818C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+94C>T ENSP00000506242.1:n.-114+94C>T