Canonical Allele Identifier: CA890067378

Gene: CRP

Linked Data

• dbSNP Id: rs1213530507
• gnomAD v3: 1-159713212-C-G
• gnomAD v4: 1-159713212-C-G
• MyVariant Identifiers: chr1:g.159683002C>G (hg19) ; chr1:g.159713212C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713212C>G , CM000663.2:g.159713212C>G	GRCh38
NC_000001.10:g.159683002C>G , CM000663.1:g.159683002C>G	GRCh37
NC_000001.9:g.157949626C>G	NCBI36
NG_013007.1:g.6378G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*313G>C MANE Select	ENSP00000255030.5:n.*313G>C
ENST00000368110.1:c.*22+291G>C	ENSP00000357091.1:n.*22+291G>C
ENST00000368111.5:c.*22+291G>C	ENSP00000357092.1:n.*22+291G>C
ENST00000368112.5:c.*22+291G>C	ENSP00000357093.1:n.*22+291G>C
ENST00000437342.1:c.*22+291G>C	ENSP00000402788.1:n.*22+291G>C
ENST00000473196.1:n.265+291G>C
ENST00000489317.1:n.75-418G>C
NM_000567.2:c.*313G>C	NP_000558.2:n.*313G>C
XM_011509207.1:c.*22+291G>C	XP_011507509.1:n.*22+291G>C
NM_001329057.1:c.*22+291G>C	NP_001315986.1:n.*22+291G>C
NM_001329058.1:c.*22+291G>C	NP_001315987.1:n.*22+291G>C
NM_000567.3:c.*313G>C MANE Select	NP_000558.2:n.*313G>C
NM_001329057.2:c.*22+291G>C	NP_001315986.1:n.*22+291G>C
NM_001329058.2:c.*22+291G>C	NP_001315987.1:n.*22+291G>C
NM_001382703.1:c.*313G>C	NP_001369632.1:n.*313G>C