Canonical Allele Identifier: CA422374022
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1571813553
gnomAD v3: 1-186680766-T-A
gnomAD v4: 1-186680766-T-A
MyVariant Identifiers: chr1:g.186649898T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680766T>A , CM000663.2:g.186680766T>A GRCh38
NC_000001.10:g.186649898T>A , CM000663.1:g.186649898T>A GRCh37
NC_000001.9:g.184916521T>A NCBI36
NG_028206.2:g.4662A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-176A>T (PTGS2) ENSP00000506242.1:n.-176A>T
NR_125801.1:n.113T>A (PACERR)
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