Canonical Allele Identifier: CA422374451
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186650038G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680906G>A , CM000663.2:g.186680906G>A GRCh38
NC_000001.10:g.186650038G>A , CM000663.1:g.186650038G>A GRCh37
NC_000001.9:g.184916661G>A NCBI36
NG_028206.2:g.4522C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-316C>T (PTGS2) ENSP00000506242.1:n.-316C>T
NR_125801.1:n.253G>A (PACERR)