Canonical Allele Identifier: CA1213243935
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673756A= , CM000663.2:g.186673756A= GRCh38
NC_000001.10:g.186642888A= , CM000663.1:g.186642888A= GRCh37
NC_000001.9:g.184909511A= NCBI36
NG_028206.2:g.11672T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*597T= MANE Select ENSP00000356438.5:n.*597T=
ENST00000680451.1:c.*597T= ENSP00000506242.1:n.*597T=
ENST00000681605.1:c.*2084T= ENSP00000504900.1:n.*2084T=
ENST00000367468.9:c.*597T= ENSP00000356438.5:n.*597T=
ENST00000490885.6:n.2827T=
NM_000963.3:c.*597T= NP_000954.1:n.*597T=
NM_000963.4:c.*597T= MANE Select NP_000954.1:n.*597T=