Canonical Allele Identifier: CA422374478
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186650047G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680915G>T , CM000663.2:g.186680915G>T GRCh38
NC_000001.10:g.186650047G>T , CM000663.1:g.186650047G>T GRCh37
NC_000001.9:g.184916670G>T NCBI36
NG_028206.2:g.4513C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-325C>A (PTGS2) ENSP00000506242.1:n.-325C>A
NR_125801.1:n.262G>T (PACERR)