Canonical Allele Identifier: CA890066894

Gene: CRP

Linked Data

• dbSNP Id: rs1414231029
• gnomAD v4: 1-159712461-C-A
• MyVariant Identifiers: chr1:g.159682251C>A (hg19) ; chr1:g.159712461C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712461C>A , CM000663.2:g.159712461C>A	GRCh38
NC_000001.10:g.159682251C>A , CM000663.1:g.159682251C>A	GRCh37
NC_000001.9:g.157948875C>A	NCBI36
NG_013007.1:g.7129G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1064G>T MANE Select	ENSP00000255030.5:n.*1064G>T
ENST00000368112.5:c.*356G>T	ENSP00000357093.1:n.*356G>T
ENST00000437342.1:c.*356G>T	ENSP00000402788.1:n.*356G>T
ENST00000473196.1:n.599G>T
NM_000567.2:c.*1064G>T	NP_000558.2:n.*1064G>T
XM_011509207.1:c.*356G>T	XP_011507509.1:n.*356G>T
NM_001329057.1:c.*356G>T	NP_001315986.1:n.*356G>T
NM_001329058.1:c.*130G>T	NP_001315987.1:n.*130G>T
NM_000567.3:c.*1064G>T MANE Select	NP_000558.2:n.*1064G>T
NM_001329057.2:c.*356G>T	NP_001315986.1:n.*356G>T
NM_001329058.2:c.*130G>T	NP_001315987.1:n.*130G>T
NM_001382703.1:c.*1064G>T	NP_001369632.1:n.*1064G>T