Canonical Allele Identifier: CA422374298
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649985C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680853C>A , CM000663.2:g.186680853C>A GRCh38
NC_000001.10:g.186649985C>A , CM000663.1:g.186649985C>A GRCh37
NC_000001.9:g.184916608C>A NCBI36
NG_028206.2:g.4575G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-263G>T (PTGS2) ENSP00000506242.1:n.-263G>T
NR_125801.1:n.200C>A (PACERR)