Canonical Allele Identifier: CA890069485

Gene: CRP

Linked Data

• dbSNP Id: rs1188826085
• gnomAD v4: 1-159714600-C-T
• MyVariant Identifiers: chr1:g.159684390C>T (hg19) ; chr1:g.159714600C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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