Canonical Allele Identifier: CA31390563

Gene: CRP

Linked Data

• ClinVar Variation Id: 752112
• ClinVar RCV Id: RCV000929232
• dbSNP Id: rs978798116
• gnomAD v4: 1-159713564-C-A
• MyVariant Identifiers: chr1:g.159683354C>A (hg19) ; chr1:g.159713564C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713564C>A , CM000663.2:g.159713564C>A	GRCh38
NC_000001.10:g.159683354C>A , CM000663.1:g.159683354C>A	GRCh37
NC_000001.9:g.157949978C>A	NCBI36
NG_013007.1:g.6026G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.636G>T MANE Select	ENSP00000255030.5:p.Val212=
ENST00000368110.1:c.270G>T	ENSP00000357091.1:p.Val90=
ENST00000368111.5:c.270G>T	ENSP00000357092.1:p.Val90=
ENST00000368112.5:c.237G>T	ENSP00000357093.1:p.Val79=
ENST00000437342.1:c.102G>T	ENSP00000402788.1:p.Val34=
ENST00000473196.1:n.204G>T
ENST00000489317.1:n.74+443G>T
NM_000567.2:c.636G>T	NP_000558.2:p.Val212=
XM_011509207.1:c.636G>T	XP_011507509.1:p.Val212=
NM_001329057.1:c.636G>T	NP_001315986.1:p.Val212=
NM_001329058.1:c.237G>T	NP_001315987.1:p.Val79=
NM_000567.3:c.636G>T MANE Select	NP_000558.2:p.Val212=
NM_001329057.2:c.636G>T	NP_001315986.1:p.Val212=
NM_001329058.2:c.237G>T	NP_001315987.1:p.Val79=
NM_001382703.1:c.270G>T	NP_001369632.1:p.Val90=