Canonical Allele Identifier: CA16068047
Gene: CRP HGNC NCBI

Linked Data

dbSNP Id: rs1130864

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713301G>A , CM000663.2:g.159713301G>A GRCh38
NC_000001.10:g.159683091G>A , CM000663.1:g.159683091G>A GRCh37
NC_000001.9:g.157949715G>A NCBI36
NG_013007.1:g.6289C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*224C>T MANE Select ENSP00000255030.5:n.*224C>T
ENST00000368110.1:c.*22+202C>T ENSP00000357091.1:n.*22+202C>T
ENST00000368111.5:c.*22+202C>T ENSP00000357092.1:n.*22+202C>T
ENST00000368112.5:c.*22+202C>T ENSP00000357093.1:n.*22+202C>T
ENST00000437342.1:c.*22+202C>T ENSP00000402788.1:n.*22+202C>T
ENST00000473196.1:n.265+202C>T
ENST00000489317.1:n.75-507C>T
NM_000567.2:c.*224C>T NP_000558.2:n.*224C>T
XM_011509207.1:c.*22+202C>T XP_011507509.1:n.*22+202C>T
NM_001329057.1:c.*22+202C>T NP_001315986.1:n.*22+202C>T
NM_001329058.1:c.*22+202C>T NP_001315987.1:n.*22+202C>T
NM_000567.3:c.*224C>T MANE Select NP_000558.2:n.*224C>T
NM_001329057.2:c.*22+202C>T NP_001315986.1:n.*22+202C>T
NM_001329058.2:c.*22+202C>T NP_001315987.1:n.*22+202C>T
NM_001382703.1:c.*224C>T NP_001369632.1:n.*224C>T