Canonical Allele Identifier: CA1213245695
Gene: PTGS2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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