Canonical Allele Identifier: CA1213245359
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679727G= , CM000663.2:g.186679727G= GRCh38
NC_000001.10:g.186648859G= , CM000663.1:g.186648859G= GRCh37
NC_000001.9:g.184915482G= NCBI36
NG_028206.2:g.5701C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-289C= MANE Select ENSP00000356438.5:n.53-289C=
ENST00000680451.1:c.53-289C= ENSP00000506242.1:n.53-289C=
ENST00000681605.1:c.53-289C= ENSP00000504900.1:n.53-289C=
ENST00000367468.9:c.53-289C= ENSP00000356438.5:n.53-289C=
ENST00000490885.6:n.186-289C=
ENST00000559627.1:c.53-289C= ENSP00000454130.1:n.53-289C=
ENST00000559800.1:n.186-289C=
NM_000963.3:c.53-289C= NP_000954.1:n.53-289C=
NM_000963.4:c.53-289C= MANE Select NP_000954.1:n.53-289C=
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