Canonical Allele Identifier: CA2649583449
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680605-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680605A>C , CM000663.2:g.186680605A>C GRCh38
NC_000001.10:g.186649737A>C , CM000663.1:g.186649737A>C GRCh37
NC_000001.9:g.184916360A>C NCBI36
NG_028206.2:g.4823T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+99T>G ENSP00000506242.1:n.-114+99T>G
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