Canonical Allele Identifier: CA34081811
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs975617247
gnomAD v2: 1-186643002-T-G
gnomAD v3: 1-186673870-T-G
gnomAD v4: 1-186673870-T-G
MyVariant Identifiers: chr1:g.186643002T>G (hg19) chr1:g.186673870T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673870T>G , CM000663.2:g.186673870T>G GRCh38
NC_000001.10:g.186643002T>G , CM000663.1:g.186643002T>G GRCh37
NC_000001.9:g.184909625T>G NCBI36
NG_028206.2:g.11558A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*483A>C MANE Select ENSP00000356438.5:n.*483A>C
ENST00000680451.1:c.*483A>C ENSP00000506242.1:n.*483A>C
ENST00000681605.1:c.*1970A>C ENSP00000504900.1:n.*1970A>C
ENST00000367468.9:c.*483A>C ENSP00000356438.5:n.*483A>C
ENST00000490885.6:n.2713A>C
NM_000963.3:c.*483A>C NP_000954.1:n.*483A>C
NM_000963.4:c.*483A>C MANE Select NP_000954.1:n.*483A>C
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