Canonical Allele Identifier: CA1189125

Gene: CRP

Linked Data

• dbSNP Id: rs752667032
• ExAC: 1:159683290 T / G
• gnomAD v2: 1-159683290-T-G
• gnomAD v3: 1-159713500-T-G
• gnomAD v4: 1-159713500-T-G
• MyVariant Identifiers: chr1:g.159683290T>G (hg19) ; chr1:g.159713500T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713500T>G , CM000663.2:g.159713500T>G	GRCh38
NC_000001.10:g.159683290T>G , CM000663.1:g.159683290T>G	GRCh37
NC_000001.9:g.157949914T>G	NCBI36
NG_013007.1:g.6090A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*25A>C MANE Select	ENSP00000255030.5:n.*25A>C
ENST00000368110.1:c.*22+3A>C	ENSP00000357091.1:n.*22+3A>C
ENST00000368111.5:c.*22+3A>C	ENSP00000357092.1:n.*22+3A>C
ENST00000368112.5:c.*22+3A>C	ENSP00000357093.1:n.*22+3A>C
ENST00000437342.1:c.*22+3A>C	ENSP00000402788.1:n.*22+3A>C
ENST00000473196.1:n.265+3A>C
ENST00000489317.1:n.74+507A>C
NM_000567.2:c.*25A>C	NP_000558.2:n.*25A>C
XM_011509207.1:c.*22+3A>C	XP_011507509.1:n.*22+3A>C
NM_001329057.1:c.*22+3A>C	NP_001315986.1:n.*22+3A>C
NM_001329058.1:c.*22+3A>C	NP_001315987.1:n.*22+3A>C
NM_000567.3:c.*25A>C MANE Select	NP_000558.2:n.*25A>C
NM_001329057.2:c.*22+3A>C	NP_001315986.1:n.*22+3A>C
NM_001329058.2:c.*22+3A>C	NP_001315987.1:n.*22+3A>C
NM_001382703.1:c.*25A>C	NP_001369632.1:n.*25A>C