Canonical Allele Identifier: CA31390424

Gene: CRP

Linked Data

• dbSNP Id: rs992800659
• gnomAD v3: 1-159713317-A-G
• gnomAD v4: 1-159713317-A-G
• MyVariant Identifiers: chr1:g.159683107A>G (hg19) ; chr1:g.159713317A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713317A>G , CM000663.2:g.159713317A>G	GRCh38
NC_000001.10:g.159683107A>G , CM000663.1:g.159683107A>G	GRCh37
NC_000001.9:g.157949731A>G	NCBI36
NG_013007.1:g.6273T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*208T>C MANE Select	ENSP00000255030.5:n.*208T>C
ENST00000368110.1:c.*22+186T>C	ENSP00000357091.1:n.*22+186T>C
ENST00000368111.5:c.*22+186T>C	ENSP00000357092.1:n.*22+186T>C
ENST00000368112.5:c.*22+186T>C	ENSP00000357093.1:n.*22+186T>C
ENST00000437342.1:c.*22+186T>C	ENSP00000402788.1:n.*22+186T>C
ENST00000473196.1:n.265+186T>C
ENST00000489317.1:n.75-523T>C
NM_000567.2:c.*208T>C	NP_000558.2:n.*208T>C
XM_011509207.1:c.*22+186T>C	XP_011507509.1:n.*22+186T>C
NM_001329057.1:c.*22+186T>C	NP_001315986.1:n.*22+186T>C
NM_001329058.1:c.*22+186T>C	NP_001315987.1:n.*22+186T>C
NM_000567.3:c.*208T>C MANE Select	NP_000558.2:n.*208T>C
NM_001329057.2:c.*22+186T>C	NP_001315986.1:n.*22+186T>C
NM_001329058.2:c.*22+186T>C	NP_001315987.1:n.*22+186T>C
NM_001382703.1:c.*208T>C	NP_001369632.1:n.*208T>C