Canonical Allele Identifier: CA34081800
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs201842290
MyVariant Identifiers: chr1:g.186642904T>A (hg19) chr1:g.186673772T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673772T>A , CM000663.2:g.186673772T>A GRCh38
NC_000001.10:g.186642904T>A , CM000663.1:g.186642904T>A GRCh37
NC_000001.9:g.184909527T>A NCBI36
NG_028206.2:g.11656A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*581A>T MANE Select ENSP00000356438.5:n.*581A>T
ENST00000680451.1:c.*581A>T ENSP00000506242.1:n.*581A>T
ENST00000681605.1:c.*2068A>T ENSP00000504900.1:n.*2068A>T
ENST00000367468.9:c.*581A>T ENSP00000356438.5:n.*581A>T
ENST00000490885.6:n.2811A>T
NM_000963.3:c.*581A>T NP_000954.1:n.*581A>T
NM_000963.4:c.*581A>T MANE Select NP_000954.1:n.*581A>T
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