Canonical Allele Identifier: CA1213245286
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679551G= , CM000663.2:g.186679551G= GRCh38
NC_000001.10:g.186648683G= , CM000663.1:g.186648683G= GRCh37
NC_000001.9:g.184915306G= NCBI36
NG_028206.2:g.5877C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-113C= MANE Select ENSP00000356438.5:n.53-113C=
ENST00000680451.1:c.53-113C= ENSP00000506242.1:n.53-113C=
ENST00000681605.1:c.53-113C= ENSP00000504900.1:n.53-113C=
ENST00000367468.9:c.53-113C= ENSP00000356438.5:n.53-113C=
ENST00000490885.6:n.186-113C=
ENST00000559627.1:c.53-113C= ENSP00000454130.1:n.53-113C=
ENST00000559800.1:n.186-113C=
NM_000963.3:c.53-113C= NP_000954.1:n.53-113C=
NM_000963.4:c.53-113C= MANE Select NP_000954.1:n.53-113C=
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