Canonical Allele Identifier: CA2649583440
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680592-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680592G>T , CM000663.2:g.186680592G>T GRCh38
NC_000001.10:g.186649724G>T , CM000663.1:g.186649724G>T GRCh37
NC_000001.9:g.184916347G>T NCBI36
NG_028206.2:g.4836C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+112C>A ENSP00000506242.1:n.-114+112C>A
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