Canonical Allele Identifier: CA1213243301
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186672626T= , CM000663.2:g.186672626T= GRCh38
NC_000001.10:g.186641758T= , CM000663.1:g.186641758T= GRCh37
NC_000001.9:g.184908381T= NCBI36
NG_028206.2:g.12802A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*1727A= MANE Select ENSP00000356438.5:n.*1727A=
ENST00000680451.1:c.*1727A= ENSP00000506242.1:n.*1727A=
ENST00000681605.1:c.*3214A= ENSP00000504900.1:n.*3214A=
ENST00000367468.9:c.*1727A= ENSP00000356438.5:n.*1727A=
NM_000963.3:c.*1727A= NP_000954.1:n.*1727A=
NM_000963.4:c.*1727A= MANE Select NP_000954.1:n.*1727A=