Canonical Allele Identifier: CA1189199

Gene: CRP

Linked Data

• dbSNP Id: rs748629705
• ExAC: 1:159683637 C / T
• gnomAD v2: 1-159683637-C-T
• gnomAD v3: 1-159713847-C-T
• gnomAD v4: 1-159713847-C-T
• MyVariant Identifiers: chr1:g.159683637C>T (hg19) ; chr1:g.159713847C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713847C>T , CM000663.2:g.159713847C>T	GRCh38
NC_000001.10:g.159683637C>T , CM000663.1:g.159683637C>T	GRCh37
NC_000001.9:g.157950261C>T	NCBI36
NG_013007.1:g.5743G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.353G>A MANE Select	ENSP00000255030.5:p.Trp118Ter
ENST00000368110.1:c.193+160G>A	ENSP00000357091.1:n.193+160G>A
ENST00000368111.5:c.193+160G>A	ENSP00000357092.1:n.193+160G>A
ENST00000368112.5:c.197+156G>A	ENSP00000357093.1:n.197+156G>A
ENST00000437342.1:c.-182G>A	ENSP00000402788.1:n.-182G>A
ENST00000489317.1:n.74+160G>A
NM_000567.2:c.353G>A	NP_000558.2:p.Trp118Ter
XM_011509207.1:c.353G>A	XP_011507509.1:p.Trp118Ter
NM_001329057.1:c.353G>A	NP_001315986.1:p.Trp118Ter
NM_001329058.1:c.197+156G>A	NP_001315987.1:n.197+156G>A
NM_000567.3:c.353G>A MANE Select	NP_000558.2:p.Trp118Ter
NM_001329057.2:c.353G>A	NP_001315986.1:p.Trp118Ter
NM_001329058.2:c.197+156G>A	NP_001315987.1:n.197+156G>A
NM_001382703.1:c.193+160G>A	NP_001369632.1:n.193+160G>A