Canonical Allele Identifier: CA1213243964
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673829G= , CM000663.2:g.186673829G= GRCh38
NC_000001.10:g.186642961G= , CM000663.1:g.186642961G= GRCh37
NC_000001.9:g.184909584G= NCBI36
NG_028206.2:g.11599C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*524C= MANE Select ENSP00000356438.5:n.*524C=
ENST00000680451.1:c.*524C= ENSP00000506242.1:n.*524C=
ENST00000681605.1:c.*2011C= ENSP00000504900.1:n.*2011C=
ENST00000367468.9:c.*524C= ENSP00000356438.5:n.*524C=
ENST00000490885.6:n.2754C=
NM_000963.3:c.*524C= NP_000954.1:n.*524C=
NM_000963.4:c.*524C= MANE Select NP_000954.1:n.*524C=