Canonical Allele Identifier: CA1213243971
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673843G= , CM000663.2:g.186673843G= GRCh38
NC_000001.10:g.186642975G= , CM000663.1:g.186642975G= GRCh37
NC_000001.9:g.184909598G= NCBI36
NG_028206.2:g.11585C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*510C= MANE Select ENSP00000356438.5:n.*510C=
ENST00000680451.1:c.*510C= ENSP00000506242.1:n.*510C=
ENST00000681605.1:c.*1997C= ENSP00000504900.1:n.*1997C=
ENST00000367468.9:c.*510C= ENSP00000356438.5:n.*510C=
ENST00000490885.6:n.2740C=
NM_000963.3:c.*510C= NP_000954.1:n.*510C=
NM_000963.4:c.*510C= MANE Select NP_000954.1:n.*510C=