Canonical Allele Identifier: CA2648594192
Gene: CRP HGNC NCBI

Linked Data

gnomAD v4: 1-159714606-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714606G>T , CM000663.2:g.159714606G>T GRCh38
NC_000001.10:g.159684396G>T , CM000663.1:g.159684396G>T GRCh37
NC_000001.9:g.157951020G>T NCBI36
NG_013007.1:g.4984C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011509207.1:c.-121C>A XP_011507509.1:n.-121C>A
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