Canonical Allele Identifier: CA1008297661
Gene: CRP HGNC NCBI

Linked Data

dbSNP Id: rs1660689980
gnomAD v3: 1-159712349-C-G
gnomAD v4: 1-159712349-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712349C>G , CM000663.2:g.159712349C>G GRCh38
NC_000001.10:g.159682139C>G , CM000663.1:g.159682139C>G GRCh37
NC_000001.9:g.157948763C>G NCBI36
NG_013007.1:g.7241G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1176G>C MANE Select ENSP00000255030.5:n.*1176G>C
ENST00000437342.1:c.*468G>C ENSP00000402788.1:n.*468G>C
ENST00000473196.1:n.711G>C
NM_000567.2:c.*1176G>C NP_000558.2:n.*1176G>C
XM_011509207.1:c.*468G>C XP_011507509.1:n.*468G>C
NM_001329057.1:c.*468G>C NP_001315986.1:n.*468G>C
NM_001329058.1:c.*242G>C NP_001315987.1:n.*242G>C
NM_000567.3:c.*1176G>C MANE Select NP_000558.2:n.*1176G>C
NM_001329057.2:c.*468G>C NP_001315986.1:n.*468G>C
NM_001329058.2:c.*242G>C NP_001315987.1:n.*242G>C
NM_001382703.1:c.*1176G>C NP_001369632.1:n.*1176G>C
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