Canonical Allele Identifier: CA1189184

Gene: CRP

Linked Data

• dbSNP Id: rs763165928
• ExAC: 1:159683585 C / T
• gnomAD v2: 1-159683585-C-T
• gnomAD v4: 1-159713795-C-T
• MyVariant Identifiers: chr1:g.159683585C>T (hg19) ; chr1:g.159713795C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713795C>T , CM000663.2:g.159713795C>T	GRCh38
NC_000001.10:g.159683585C>T , CM000663.1:g.159683585C>T	GRCh37
NC_000001.9:g.157950209C>T	NCBI36
NG_013007.1:g.5795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.405G>A MANE Select	ENSP00000255030.5:p.Val135=
ENST00000368110.1:c.194-155G>A	ENSP00000357091.1:n.194-155G>A
ENST00000368111.5:c.194-155G>A	ENSP00000357092.1:n.194-155G>A
ENST00000368112.5:c.198-192G>A	ENSP00000357093.1:n.198-192G>A
ENST00000437342.1:c.-130G>A	ENSP00000402788.1:n.-130G>A
ENST00000489317.1:n.74+212G>A
NM_000567.2:c.405G>A	NP_000558.2:p.Val135=
XM_011509207.1:c.405G>A	XP_011507509.1:p.Val135=
NM_001329057.1:c.405G>A	NP_001315986.1:p.Val135=
NM_001329058.1:c.198-192G>A	NP_001315987.1:n.198-192G>A
NM_000567.3:c.405G>A MANE Select	NP_000558.2:p.Val135=
NM_001329057.2:c.405G>A	NP_001315986.1:p.Val135=
NM_001329058.2:c.198-192G>A	NP_001315987.1:n.198-192G>A
NM_001382703.1:c.194-155G>A	NP_001369632.1:n.194-155G>A