Canonical Allele Identifier: CA1213243976
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665733045

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673853T>A , CM000663.2:g.186673853T>A GRCh38
NC_000001.10:g.186642985T>A , CM000663.1:g.186642985T>A GRCh37
NC_000001.9:g.184909608T>A NCBI36
NG_028206.2:g.11575A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*500A>T MANE Select ENSP00000356438.5:n.*500A>T
ENST00000680451.1:c.*500A>T ENSP00000506242.1:n.*500A>T
ENST00000681605.1:c.*1987A>T ENSP00000504900.1:n.*1987A>T
ENST00000367468.9:c.*500A>T ENSP00000356438.5:n.*500A>T
ENST00000490885.6:n.2730A>T
NM_000963.3:c.*500A>T NP_000954.1:n.*500A>T
NM_000963.4:c.*500A>T MANE Select NP_000954.1:n.*500A>T