Canonical Allele Identifier: CA422374428
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186650030G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680898G>C , CM000663.2:g.186680898G>C GRCh38
NC_000001.10:g.186650030G>C , CM000663.1:g.186650030G>C GRCh37
NC_000001.9:g.184916653G>C NCBI36
NG_028206.2:g.4530C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-308C>G (PTGS2) ENSP00000506242.1:n.-308C>G
NR_125801.1:n.245G>C (PACERR)