Canonical Allele Identifier: CA1213243951
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673794T= , CM000663.2:g.186673794T= GRCh38
NC_000001.10:g.186642926T= , CM000663.1:g.186642926T= GRCh37
NC_000001.9:g.184909549T= NCBI36
NG_028206.2:g.11634A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*559A= MANE Select ENSP00000356438.5:n.*559A=
ENST00000680451.1:c.*559A= ENSP00000506242.1:n.*559A=
ENST00000681605.1:c.*2046A= ENSP00000504900.1:n.*2046A=
ENST00000367468.9:c.*559A= ENSP00000356438.5:n.*559A=
ENST00000490885.6:n.2789A=
NM_000963.3:c.*559A= NP_000954.1:n.*559A=
NM_000963.4:c.*559A= MANE Select NP_000954.1:n.*559A=