Canonical Allele Identifier: CA2649583450
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680608-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680608C>A , CM000663.2:g.186680608C>A GRCh38
NC_000001.10:g.186649740C>A , CM000663.1:g.186649740C>A GRCh37
NC_000001.9:g.184916363C>A NCBI36
NG_028206.2:g.4820G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+96G>T ENSP00000506242.1:n.-114+96G>T
Search 100 bp 5'
Search 100 bp 3'