Canonical Allele Identifier: CA1189303

Gene: CRP

Linked Data

• dbSNP Id: rs777480636
• ExAC: 1:159684274 A / G
• gnomAD v2: 1-159684274-A-G
• gnomAD v3: 1-159714484-A-G
• gnomAD v4: 1-159714484-A-G
• MyVariant Identifiers: chr1:g.159684274A>G (hg19) ; chr1:g.159714484A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714484A>G , CM000663.2:g.159714484A>G	GRCh38
NC_000001.10:g.159684274A>G , CM000663.1:g.159684274A>G	GRCh37
NC_000001.9:g.157950898A>G	NCBI36
NG_013007.1:g.5106T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.2T>C MANE Select	ENSP00000255030.5:p.Met1Thr
ENST00000368110.1:c.2T>C	ENSP00000357091.1:p.Met1Thr
ENST00000368111.5:c.2T>C	ENSP00000357092.1:p.Met1Thr
ENST00000368112.5:c.2T>C	ENSP00000357093.1:p.Met1Thr
ENST00000437342.1:c.-308+15T>C	ENSP00000402788.1:n.-308+15T>C
NM_000567.2:c.2T>C	NP_000558.2:p.Met1Thr
XM_011509207.1:c.2T>C	XP_011507509.1:p.Met1Thr
NM_001329057.1:c.2T>C	NP_001315986.1:p.Met1Thr
NM_001329058.1:c.2T>C	NP_001315987.1:p.Met1Thr
NM_000567.3:c.2T>C MANE Select	NP_000558.2:p.Met1Thr
NM_001329057.2:c.2T>C	NP_001315986.1:p.Met1Thr
NM_001329058.2:c.2T>C	NP_001315987.1:p.Met1Thr
NM_001382703.1:c.2T>C	NP_001369632.1:p.Met1Thr