Canonical Allele Identifier: CA2648594187
Gene: CRP HGNC NCBI

Linked Data

gnomAD v4: 1-159714601-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714601C>A , CM000663.2:g.159714601C>A GRCh38
NC_000001.10:g.159684391C>A , CM000663.1:g.159684391C>A GRCh37
NC_000001.9:g.157951015C>A NCBI36
NG_013007.1:g.4989G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-116G>T XP_011507509.1:n.-116G>T
Search 100 bp 5'
Search 100 bp 3'