Canonical Allele Identifier: CA1189196

Gene: CRP

Linked Data

• dbSNP Id: rs745569100
• ExAC: 1:159683626 A / C
• gnomAD v2: 1-159683626-A-C
• gnomAD v4: 1-159713836-A-C
• MyVariant Identifiers: chr1:g.159683626A>C (hg19) ; chr1:g.159713836A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713836A>C , CM000663.2:g.159713836A>C	GRCh38
NC_000001.10:g.159683626A>C , CM000663.1:g.159683626A>C	GRCh37
NC_000001.9:g.157950250A>C	NCBI36
NG_013007.1:g.5754T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.364T>G MANE Select	ENSP00000255030.5:p.Ser122Ala
ENST00000368110.1:c.193+171T>G	ENSP00000357091.1:n.193+171T>G
ENST00000368111.5:c.193+171T>G	ENSP00000357092.1:n.193+171T>G
ENST00000368112.5:c.197+167T>G	ENSP00000357093.1:n.197+167T>G
ENST00000437342.1:c.-171T>G	ENSP00000402788.1:n.-171T>G
ENST00000489317.1:n.74+171T>G
NM_000567.2:c.364T>G	NP_000558.2:p.Ser122Ala
XM_011509207.1:c.364T>G	XP_011507509.1:p.Ser122Ala
NM_001329057.1:c.364T>G	NP_001315986.1:p.Ser122Ala
NM_001329058.1:c.197+167T>G	NP_001315987.1:n.197+167T>G
NM_000567.3:c.364T>G MANE Select	NP_000558.2:p.Ser122Ala
NM_001329057.2:c.364T>G	NP_001315986.1:p.Ser122Ala
NM_001329058.2:c.197+167T>G	NP_001315987.1:n.197+167T>G
NM_001382703.1:c.193+171T>G	NP_001369632.1:n.193+171T>G