Canonical Allele Identifier: CA2649583508
Gene: PTGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679529T>A , CM000663.2:g.186679529T>A GRCh38
NC_000001.10:g.186648661T>A , CM000663.1:g.186648661T>A GRCh37
NC_000001.9:g.184915284T>A NCBI36
NG_028206.2:g.5899A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-91A>T MANE Select ENSP00000356438.5:n.53-91A>T
ENST00000680451.1:c.53-91A>T ENSP00000506242.1:n.53-91A>T
ENST00000681605.1:c.53-91A>T ENSP00000504900.1:n.53-91A>T
ENST00000367468.9:c.53-91A>T ENSP00000356438.5:n.53-91A>T
ENST00000490885.6:n.186-91A>T
ENST00000559627.1:c.53-91A>T ENSP00000454130.1:n.53-91A>T
ENST00000559800.1:n.186-91A>T
NM_000963.3:c.53-91A>T NP_000954.1:n.53-91A>T
NM_000963.4:c.53-91A>T MANE Select NP_000954.1:n.53-91A>T