Canonical Allele Identifier: CA2649583328
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680503-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680503T>C , CM000663.2:g.186680503T>C GRCh38
NC_000001.10:g.186649635T>C , CM000663.1:g.186649635T>C GRCh37
NC_000001.9:g.184916258T>C NCBI36
NG_028206.2:g.4925A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-100A>G ENSP00000506242.1:n.-113-100A>G
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