Canonical Allele Identifier: CA890069486

Gene: CRP

Linked Data

• dbSNP Id: rs1259701529
• gnomAD v3: 1-159714599-TC-T
• gnomAD v4: 1-159714599-TC-T
• MyVariant Identifiers: chr1:g.159684390del (hg19) ; chr1:g.159714600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714601del , CM000663.2:g.159714601del	GRCh38
NC_000001.10:g.159684391del , CM000663.1:g.159684391del	GRCh37
NC_000001.9:g.157951015del	NCBI36
NG_013007.1:g.4990del

Transcript Alleles

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