Canonical Allele Identifier: CA1213244005
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673912G= , CM000663.2:g.186673912G= GRCh38
NC_000001.10:g.186643044G= , CM000663.1:g.186643044G= GRCh37
NC_000001.9:g.184909667G= NCBI36
NG_028206.2:g.11516C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*441C= MANE Select ENSP00000356438.5:n.*441C=
ENST00000680451.1:c.*441C= ENSP00000506242.1:n.*441C=
ENST00000681605.1:c.*1928C= ENSP00000504900.1:n.*1928C=
ENST00000367468.9:c.*441C= ENSP00000356438.5:n.*441C=
ENST00000490885.6:n.2671C=
NM_000963.3:c.*441C= NP_000954.1:n.*441C=
NM_000963.4:c.*441C= MANE Select NP_000954.1:n.*441C=