Canonical Allele Identifier: CA2648592706
Gene: CRP HGNC NCBI

Linked Data

gnomAD v4: 1-159712289-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712289T>C , CM000663.2:g.159712289T>C GRCh38
NC_000001.10:g.159682079T>C , CM000663.1:g.159682079T>C GRCh37
NC_000001.9:g.157948703T>C NCBI36
NG_013007.1:g.7301A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1236A>G MANE Select ENSP00000255030.5:n.*1236A>G
NM_000567.2:c.*1236A>G NP_000558.2:n.*1236A>G
XM_011509207.1:c.*528A>G XP_011507509.1:n.*528A>G
NM_001329057.1:c.*528A>G NP_001315986.1:n.*528A>G
NM_001329058.1:c.*302A>G NP_001315987.1:n.*302A>G
NM_000567.3:c.*1236A>G MANE Select NP_000558.2:n.*1236A>G
NM_001329057.2:c.*528A>G NP_001315986.1:n.*528A>G
NM_001329058.2:c.*302A>G NP_001315987.1:n.*302A>G
NM_001382703.1:c.*1236A>G NP_001369632.1:n.*1236A>G
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