Canonical Allele Identifier: CA1143416373
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673818G= , CM000663.2:g.186673818G= GRCh38
NC_000001.10:g.186642950G= , CM000663.1:g.186642950G= GRCh37
NC_000001.9:g.184909573G= NCBI36
NG_028206.2:g.11610C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*535C= MANE Select ENSP00000356438.5:n.*535C=
ENST00000680451.1:c.*535C= ENSP00000506242.1:n.*535C=
ENST00000681605.1:c.*2022C= ENSP00000504900.1:n.*2022C=
ENST00000367468.9:c.*535C= ENSP00000356438.5:n.*535C=
ENST00000490885.6:n.2765C=
NM_000963.3:c.*535C= NP_000954.1:n.*535C=
NM_000963.4:c.*535C= MANE Select NP_000954.1:n.*535C=