Canonical Allele Identifier: CA422373873
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649852T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680720T>A , CM000663.2:g.186680720T>A GRCh38
NC_000001.10:g.186649852T>A , CM000663.1:g.186649852T>A GRCh37
NC_000001.9:g.184916475T>A NCBI36
NG_028206.2:g.4708A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-130A>T (PTGS2) ENSP00000506242.1:n.-130A>T
NR_125801.1:n.67T>A (PACERR)