Canonical Allele Identifier: CA2649583312
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680488-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680488C>A , CM000663.2:g.186680488C>A GRCh38
NC_000001.10:g.186649620C>A , CM000663.1:g.186649620C>A GRCh37
NC_000001.9:g.184916243C>A NCBI36
NG_028206.2:g.4940G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-85G>T ENSP00000506242.1:n.-113-85G>T
Search 100 bp 5'
Search 100 bp 3'