Canonical Allele Identifier: CA1144933815
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673822C= , CM000663.2:g.186673822C= GRCh38
NC_000001.10:g.186642954C= , CM000663.1:g.186642954C= GRCh37
NC_000001.9:g.184909577C= NCBI36
NG_028206.2:g.11606G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*531G= MANE Select ENSP00000356438.5:n.*531G=
ENST00000680451.1:c.*531G= ENSP00000506242.1:n.*531G=
ENST00000681605.1:c.*2018G= ENSP00000504900.1:n.*2018G=
ENST00000367468.9:c.*531G= ENSP00000356438.5:n.*531G=
ENST00000490885.6:n.2761G=
NM_000963.3:c.*531G= NP_000954.1:n.*531G=
NM_000963.4:c.*531G= MANE Select NP_000954.1:n.*531G=