Canonical Allele Identifier: CA1213243309
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186672635A= , CM000663.2:g.186672635A= GRCh38
NC_000001.10:g.186641767A= , CM000663.1:g.186641767A= GRCh37
NC_000001.9:g.184908390A= NCBI36
NG_028206.2:g.12793T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*1718T= MANE Select ENSP00000356438.5:n.*1718T=
ENST00000680451.1:c.*1718T= ENSP00000506242.1:n.*1718T=
ENST00000681605.1:c.*3205T= ENSP00000504900.1:n.*3205T=
ENST00000367468.9:c.*1718T= ENSP00000356438.5:n.*1718T=
NM_000963.3:c.*1718T= NP_000954.1:n.*1718T=
NM_000963.4:c.*1718T= MANE Select NP_000954.1:n.*1718T=