Canonical Allele Identifier: CA31391044

Gene: CRP

Linked Data

• dbSNP Id: rs370080304
• gnomAD v4: 1-159714595-T-C
• MyVariant Identifiers: chr1:g.159684385T>C (hg19) ; chr1:g.159714595T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714595T>C , CM000663.2:g.159714595T>C	GRCh38
NC_000001.10:g.159684385T>C , CM000663.1:g.159684385T>C	GRCh37
NC_000001.9:g.157951009T>C	NCBI36
NG_013007.1:g.4995A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011509207.1:c.-110A>G	XP_011507509.1:n.-110A>G