Canonical Allele Identifier: CA1213245754
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1558252667
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680601G>A , CM000663.2:g.186680601G>A GRCh38
NC_000001.10:g.186649733G>A , CM000663.1:g.186649733G>A GRCh37
NC_000001.9:g.184916356G>A NCBI36
NG_028206.2:g.4827C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+103C>T ENSP00000506242.1:n.-114+103C>T
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