Canonical Allele Identifier: CA2648592733
Gene: CRP HGNC NCBI

Linked Data

gnomAD v4: 1-159712345-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712345G>T , CM000663.2:g.159712345G>T GRCh38
NC_000001.10:g.159682135G>T , CM000663.1:g.159682135G>T GRCh37
NC_000001.9:g.157948759G>T NCBI36
NG_013007.1:g.7245C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1180C>A MANE Select ENSP00000255030.5:n.*1180C>A
ENST00000437342.1:c.*472C>A ENSP00000402788.1:n.*472C>A
ENST00000473196.1:n.715C>A
NM_000567.2:c.*1180C>A NP_000558.2:n.*1180C>A
XM_011509207.1:c.*472C>A XP_011507509.1:n.*472C>A
NM_001329057.1:c.*472C>A NP_001315986.1:n.*472C>A
NM_001329058.1:c.*246C>A NP_001315987.1:n.*246C>A
NM_000567.3:c.*1180C>A MANE Select NP_000558.2:n.*1180C>A
NM_001329057.2:c.*472C>A NP_001315986.1:n.*472C>A
NM_001329058.2:c.*246C>A NP_001315987.1:n.*246C>A
NM_001382703.1:c.*1180C>A NP_001369632.1:n.*1180C>A
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