Canonical Allele Identifier: CA31391046

Gene: CRP

Linked Data

• dbSNP Id: rs1006776031
• MyVariant Identifiers: chr1:g.159684393C>G (hg19) ; chr1:g.159714603C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714603C>G , CM000663.2:g.159714603C>G	GRCh38
NC_000001.10:g.159684393C>G , CM000663.1:g.159684393C>G	GRCh37
NC_000001.9:g.157951017C>G	NCBI36
NG_013007.1:g.4987G>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011509207.1:c.-118G>C	XP_011507509.1:n.-118G>C