Canonical Allele Identifier: CA343454260
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713829A>G , CM000663.2:g.159713829A>G GRCh38
NC_000001.10:g.159683619A>G , CM000663.1:g.159683619A>G GRCh37
NC_000001.9:g.157950243A>G NCBI36
NG_013007.1:g.5761T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.371T>C MANE Select ENSP00000255030.5:p.Ile124Thr
ENST00000368110.1:c.193+178T>C ENSP00000357091.1:n.193+178T>C
ENST00000368111.5:c.193+178T>C ENSP00000357092.1:n.193+178T>C
ENST00000368112.5:c.197+174T>C ENSP00000357093.1:n.197+174T>C
ENST00000437342.1:c.-164T>C ENSP00000402788.1:n.-164T>C
ENST00000489317.1:n.74+178T>C
NM_000567.2:c.371T>C NP_000558.2:p.Ile124Thr
XM_011509207.1:c.371T>C XP_011507509.1:p.Ile124Thr
NM_001329057.1:c.371T>C NP_001315986.1:p.Ile124Thr
NM_001329058.1:c.197+174T>C NP_001315987.1:n.197+174T>C
NM_000567.3:c.371T>C MANE Select NP_000558.2:p.Ile124Thr
NM_001329057.2:c.371T>C NP_001315986.1:p.Ile124Thr
NM_001329058.2:c.197+174T>C NP_001315987.1:n.197+174T>C
NM_001382703.1:c.193+178T>C NP_001369632.1:n.193+178T>C