Canonical Allele Identifier: CA1202016795
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714600C= , CM000663.2:g.159714600C= GRCh38
NC_000001.10:g.159684390C= , CM000663.1:g.159684390C= GRCh37
NC_000001.9:g.157951014C= NCBI36
NG_013007.1:g.4990G=

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-115G= XP_011507509.1:n.-115G=