Canonical Allele Identifier: CA2697645112
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs2102004215
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673885A>G , CM000663.2:g.186673885A>G GRCh38
NC_000001.10:g.186643017A>G , CM000663.1:g.186643017A>G GRCh37
NC_000001.9:g.184909640A>G NCBI36
NG_028206.2:g.11543T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*468T>C MANE Select ENSP00000356438.5:n.*468T>C
ENST00000680451.1:c.*468T>C ENSP00000506242.1:n.*468T>C
ENST00000681605.1:c.*1955T>C ENSP00000504900.1:n.*1955T>C
ENST00000367468.9:c.*468T>C ENSP00000356438.5:n.*468T>C
ENST00000490885.6:n.2698T>C
NM_000963.3:c.*468T>C NP_000954.1:n.*468T>C
NM_000963.4:c.*468T>C MANE Select NP_000954.1:n.*468T>C
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