Canonical Allele Identifier: CA2648594188
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714602T>C , CM000663.2:g.159714602T>C GRCh38
NC_000001.10:g.159684392T>C , CM000663.1:g.159684392T>C GRCh37
NC_000001.9:g.157951016T>C NCBI36
NG_013007.1:g.4988A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-117A>G XP_011507509.1:n.-117A>G