Canonical Allele Identifier: CA422373953
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs920019065
gnomAD v2: 1-186649877-C-T
gnomAD v3: 1-186680745-C-T
gnomAD v4: 1-186680745-C-T
MyVariant Identifiers: chr1:g.186649877C>T (hg19) chr1:g.186680745C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680745C>T , CM000663.2:g.186680745C>T GRCh38
NC_000001.10:g.186649877C>T , CM000663.1:g.186649877C>T GRCh37
NC_000001.9:g.184916500C>T NCBI36
NG_028206.2:g.4683G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-155G>A (PTGS2) ENSP00000506242.1:n.-155G>A
NR_125801.1:n.92C>T (PACERR)
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