Canonical Allele Identifier: CA1147715213
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680490G= , CM000663.2:g.186680490G= GRCh38
NC_000001.10:g.186649622G= , CM000663.1:g.186649622G= GRCh37
NC_000001.9:g.184916245G= NCBI36
NG_028206.2:g.4938C=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-87C= ENSP00000506242.1:n.-113-87C=