Canonical Allele Identifier: CA2648594189
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714603C>A , CM000663.2:g.159714603C>A GRCh38
NC_000001.10:g.159684393C>A , CM000663.1:g.159684393C>A GRCh37
NC_000001.9:g.157951017C>A NCBI36
NG_013007.1:g.4987G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-118G>T XP_011507509.1:n.-118G>T