Canonical Allele Identifier: CA1202016801
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714609T= , CM000663.2:g.159714609T= GRCh38
NC_000001.10:g.159684399T= , CM000663.1:g.159684399T= GRCh37
NC_000001.9:g.157951023T= NCBI36
NG_013007.1:g.4981A=

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-124A= XP_011507509.1:n.-124A=