Canonical Allele Identifier: CA890067375

Gene: CRP

Linked Data

• dbSNP Id: rs1241399098
• MyVariant Identifiers: chr1:g.159682991A>C (hg19) ; chr1:g.159713201A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713201A>C , CM000663.2:g.159713201A>C	GRCh38
NC_000001.10:g.159682991A>C , CM000663.1:g.159682991A>C	GRCh37
NC_000001.9:g.157949615A>C	NCBI36
NG_013007.1:g.6389T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*324T>G MANE Select	ENSP00000255030.5:n.*324T>G
ENST00000368110.1:c.*22+302T>G	ENSP00000357091.1:n.*22+302T>G
ENST00000368111.5:c.*22+302T>G	ENSP00000357092.1:n.*22+302T>G
ENST00000368112.5:c.*22+302T>G	ENSP00000357093.1:n.*22+302T>G
ENST00000437342.1:c.*22+302T>G	ENSP00000402788.1:n.*22+302T>G
ENST00000473196.1:n.265+302T>G
ENST00000489317.1:n.75-407T>G
NM_000567.2:c.*324T>G	NP_000558.2:n.*324T>G
XM_011509207.1:c.*22+302T>G	XP_011507509.1:n.*22+302T>G
NM_001329057.1:c.*22+302T>G	NP_001315986.1:n.*22+302T>G
NM_001329058.1:c.*22+302T>G	NP_001315987.1:n.*22+302T>G
NM_000567.3:c.*324T>G MANE Select	NP_000558.2:n.*324T>G
NM_001329057.2:c.*22+302T>G	NP_001315986.1:n.*22+302T>G
NM_001329058.2:c.*22+302T>G	NP_001315987.1:n.*22+302T>G
NM_001382703.1:c.*324T>G	NP_001369632.1:n.*324T>G