Canonical Allele Identifier: CA1202014226

Gene: CRP

Linked Data

• dbSNP Id: rs1660690898

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712363T>G , CM000663.2:g.159712363T>G	GRCh38
NC_000001.10:g.159682153T>G , CM000663.1:g.159682153T>G	GRCh37
NC_000001.9:g.157948777T>G	NCBI36
NG_013007.1:g.7227A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1162A>C MANE Select	ENSP00000255030.5:n.*1162A>C
ENST00000437342.1:c.*454A>C	ENSP00000402788.1:n.*454A>C
ENST00000473196.1:n.697A>C
NM_000567.2:c.*1162A>C	NP_000558.2:n.*1162A>C
XM_011509207.1:c.*454A>C	XP_011507509.1:n.*454A>C
NM_001329057.1:c.*454A>C	NP_001315986.1:n.*454A>C
NM_001329058.1:c.*228A>C	NP_001315987.1:n.*228A>C
NM_000567.3:c.*1162A>C MANE Select	NP_000558.2:n.*1162A>C
NM_001329057.2:c.*454A>C	NP_001315986.1:n.*454A>C
NM_001329058.2:c.*228A>C	NP_001315987.1:n.*228A>C
NM_001382703.1:c.*1162A>C	NP_001369632.1:n.*1162A>C