Canonical Allele Identifier: CA1139984986
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714591G= , CM000663.2:g.159714591G= GRCh38
NC_000001.10:g.159684381G= , CM000663.1:g.159684381G= GRCh37
NC_000001.9:g.157951005G= NCBI36
NG_013007.1:g.4999C=

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-106C= XP_011507509.1:n.-106C=