Canonical Allele Identifier: CA890067415

Gene: CRP

Linked Data

• dbSNP Id: rs1372570392
• gnomAD v3: 1-159713311-A-G
• gnomAD v4: 1-159713311-A-G
• MyVariant Identifiers: chr1:g.159683101A>G (hg19) ; chr1:g.159713311A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713311A>G , CM000663.2:g.159713311A>G	GRCh38
NC_000001.10:g.159683101A>G , CM000663.1:g.159683101A>G	GRCh37
NC_000001.9:g.157949725A>G	NCBI36
NG_013007.1:g.6279T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*214T>C MANE Select	ENSP00000255030.5:n.*214T>C
ENST00000368110.1:c.*22+192T>C	ENSP00000357091.1:n.*22+192T>C
ENST00000368111.5:c.*22+192T>C	ENSP00000357092.1:n.*22+192T>C
ENST00000368112.5:c.*22+192T>C	ENSP00000357093.1:n.*22+192T>C
ENST00000437342.1:c.*22+192T>C	ENSP00000402788.1:n.*22+192T>C
ENST00000473196.1:n.265+192T>C
ENST00000489317.1:n.75-517T>C
NM_000567.2:c.*214T>C	NP_000558.2:n.*214T>C
XM_011509207.1:c.*22+192T>C	XP_011507509.1:n.*22+192T>C
NM_001329057.1:c.*22+192T>C	NP_001315986.1:n.*22+192T>C
NM_001329058.1:c.*22+192T>C	NP_001315987.1:n.*22+192T>C
NM_000567.3:c.*214T>C MANE Select	NP_000558.2:n.*214T>C
NM_001329057.2:c.*22+192T>C	NP_001315986.1:n.*22+192T>C
NM_001329058.2:c.*22+192T>C	NP_001315987.1:n.*22+192T>C
NM_001382703.1:c.*214T>C	NP_001369632.1:n.*214T>C