Canonical Allele Identifier: CA1213243992
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673889T= , CM000663.2:g.186673889T= GRCh38
NC_000001.10:g.186643021T= , CM000663.1:g.186643021T= GRCh37
NC_000001.9:g.184909644T= NCBI36
NG_028206.2:g.11539A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*464A= MANE Select ENSP00000356438.5:n.*464A=
ENST00000680451.1:c.*464A= ENSP00000506242.1:n.*464A=
ENST00000681605.1:c.*1951A= ENSP00000504900.1:n.*1951A=
ENST00000367468.9:c.*464A= ENSP00000356438.5:n.*464A=
ENST00000490885.6:n.2694A=
NM_000963.3:c.*464A= NP_000954.1:n.*464A=
NM_000963.4:c.*464A= MANE Select NP_000954.1:n.*464A=