Canonical Allele Identifier: CA421618172

Gene: CRP

Linked Data

• dbSNP Id: rs1446491769
• gnomAD v2: 1-159683342-C-A
• gnomAD v4: 1-159713552-C-A
• COSMIC: COSM335095
• MyVariant Identifiers: chr1:g.159683342C>A (hg19) ; chr1:g.159713552C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713552C>A , CM000663.2:g.159713552C>A	GRCh38
NC_000001.10:g.159683342C>A , CM000663.1:g.159683342C>A	GRCh37
NC_000001.9:g.157949966C>A	NCBI36
NG_013007.1:g.6038G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.648G>T MANE Select	ENSP00000255030.5:p.Val216=
ENST00000368110.1:c.282G>T	ENSP00000357091.1:p.Val94=
ENST00000368111.5:c.282G>T	ENSP00000357092.1:p.Val94=
ENST00000368112.5:c.249G>T	ENSP00000357093.1:p.Val83=
ENST00000437342.1:c.114G>T	ENSP00000402788.1:p.Val38=
ENST00000473196.1:n.216G>T
ENST00000489317.1:n.74+455G>T
NM_000567.2:c.648G>T	NP_000558.2:p.Val216=
XM_011509207.1:c.648G>T	XP_011507509.1:p.Val216=
NM_001329057.1:c.648G>T	NP_001315986.1:p.Val216=
NM_001329058.1:c.249G>T	NP_001315987.1:p.Val83=
NM_000567.3:c.648G>T MANE Select	NP_000558.2:p.Val216=
NM_001329057.2:c.648G>T	NP_001315986.1:p.Val216=
NM_001329058.2:c.249G>T	NP_001315987.1:p.Val83=
NM_001382703.1:c.282G>T	NP_001369632.1:p.Val94=