Canonical Allele Identifier: CA422374012
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649894C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680762C>T , CM000663.2:g.186680762C>T GRCh38
NC_000001.10:g.186649894C>T , CM000663.1:g.186649894C>T GRCh37
NC_000001.9:g.184916517C>T NCBI36
NG_028206.2:g.4666G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-172G>A (PTGS2) ENSP00000506242.1:n.-172G>A
NR_125801.1:n.109C>T (PACERR)