Canonical Allele Identifier: CA1213245641
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680379T= , CM000663.2:g.186680379T= GRCh38
NC_000001.10:g.186649511T= , CM000663.1:g.186649511T= GRCh37
NC_000001.9:g.184916134T= NCBI36
NG_028206.2:g.5049A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-89A= MANE Select ENSP00000356438.5:n.-89A=
ENST00000680451.1:c.-89A= ENSP00000506242.1:n.-89A=
ENST00000681605.1:c.-89A= ENSP00000504900.1:n.-89A=
ENST00000367468.9:c.-89A= ENSP00000356438.5:n.-89A=
ENST00000490885.6:n.45A=
ENST00000559800.1:n.45A=
NM_000963.3:c.-89A= NP_000954.1:n.-89A=
NM_000963.4:c.-89A= MANE Select NP_000954.1:n.-89A=
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