Canonical Allele Identifier: CA2648594182
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714594C>T , CM000663.2:g.159714594C>T GRCh38
NC_000001.10:g.159684384C>T , CM000663.1:g.159684384C>T GRCh37
NC_000001.9:g.157951008C>T NCBI36
NG_013007.1:g.4996G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-109G>A XP_011507509.1:n.-109G>A