Canonical Allele Identifier: CA1213243312
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186672645G= , CM000663.2:g.186672645G= GRCh38
NC_000001.10:g.186641777G= , CM000663.1:g.186641777G= GRCh37
NC_000001.9:g.184908400G= NCBI36
NG_028206.2:g.12783C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*1708C= MANE Select ENSP00000356438.5:n.*1708C=
ENST00000680451.1:c.*1708C= ENSP00000506242.1:n.*1708C=
ENST00000681605.1:c.*3195C= ENSP00000504900.1:n.*3195C=
ENST00000367468.9:c.*1708C= ENSP00000356438.5:n.*1708C=
NM_000963.3:c.*1708C= NP_000954.1:n.*1708C=
NM_000963.4:c.*1708C= MANE Select NP_000954.1:n.*1708C=