Canonical Allele Identifier: CA1213245694
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680508G= , CM000663.2:g.186680508G= GRCh38
NC_000001.10:g.186649640G= , CM000663.1:g.186649640G= GRCh37
NC_000001.9:g.184916263G= NCBI36
NG_028206.2:g.4920C=

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-105C= ENSP00000506242.1:n.-113-105C=