Canonical Allele Identifier: CA422374455
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186650039T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680907T>G , CM000663.2:g.186680907T>G GRCh38
NC_000001.10:g.186650039T>G , CM000663.1:g.186650039T>G GRCh37
NC_000001.9:g.184916662T>G NCBI36
NG_028206.2:g.4521A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-317A>C (PTGS2) ENSP00000506242.1:n.-317A>C
NR_125801.1:n.254T>G (PACERR)
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