Canonical Allele Identifier: CA422373906
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

gnomAD v4: 1-186680730-T-G
MyVariant Identifiers: chr1:g.186649862T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680730T>G , CM000663.2:g.186680730T>G GRCh38
NC_000001.10:g.186649862T>G , CM000663.1:g.186649862T>G GRCh37
NC_000001.9:g.184916485T>G NCBI36
NG_028206.2:g.4698A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-140A>C (PTGS2) ENSP00000506242.1:n.-140A>C
NR_125801.1:n.77T>G (PACERR)
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