Canonical Allele Identifier: CA1202014218

Gene: CRP

Linked Data

• dbSNP Id: rs1051527257

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712355A>T , CM000663.2:g.159712355A>T	GRCh38
NC_000001.10:g.159682145A>T , CM000663.1:g.159682145A>T	GRCh37
NC_000001.9:g.157948769A>T	NCBI36
NG_013007.1:g.7235T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1170T>A MANE Select	ENSP00000255030.5:n.*1170T>A
ENST00000437342.1:c.*462T>A	ENSP00000402788.1:n.*462T>A
ENST00000473196.1:n.705T>A
NM_000567.2:c.*1170T>A	NP_000558.2:n.*1170T>A
XM_011509207.1:c.*462T>A	XP_011507509.1:n.*462T>A
NM_001329057.1:c.*462T>A	NP_001315986.1:n.*462T>A
NM_001329058.1:c.*236T>A	NP_001315987.1:n.*236T>A
NM_000567.3:c.*1170T>A MANE Select	NP_000558.2:n.*1170T>A
NM_001329057.2:c.*462T>A	NP_001315986.1:n.*462T>A
NM_001329058.2:c.*236T>A	NP_001315987.1:n.*236T>A
NM_001382703.1:c.*1170T>A	NP_001369632.1:n.*1170T>A