Canonical Allele Identifier: CA1189212

Gene: CRP

Linked Data

• ClinVar Variation Id: 3077627
• ClinVar RCV Id: RCV004369957
• dbSNP Id: rs753340450
• ExAC: 1:159683688 A / G
• gnomAD v2: 1-159683688-A-G
• gnomAD v3: 1-159713898-A-G
• gnomAD v4: 1-159713898-A-G
• MyVariant Identifiers: chr1:g.159683688A>G (hg19) ; chr1:g.159713898A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713898A>G , CM000663.2:g.159713898A>G	GRCh38
NC_000001.10:g.159683688A>G , CM000663.1:g.159683688A>G	GRCh37
NC_000001.9:g.157950312A>G	NCBI36
NG_013007.1:g.5692T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.302T>C MANE Select	ENSP00000255030.5:p.Leu101Ser
ENST00000368110.1:c.193+109T>C	ENSP00000357091.1:n.193+109T>C
ENST00000368111.5:c.193+109T>C	ENSP00000357092.1:n.193+109T>C
ENST00000368112.5:c.197+105T>C	ENSP00000357093.1:n.197+105T>C
ENST00000437342.1:c.-233T>C	ENSP00000402788.1:n.-233T>C
ENST00000489317.1:n.74+109T>C
NM_000567.2:c.302T>C	NP_000558.2:p.Leu101Ser
XM_011509207.1:c.302T>C	XP_011507509.1:p.Leu101Ser
NM_001329057.1:c.302T>C	NP_001315986.1:p.Leu101Ser
NM_001329058.1:c.197+105T>C	NP_001315987.1:n.197+105T>C
NM_000567.3:c.302T>C MANE Select	NP_000558.2:p.Leu101Ser
NM_001329057.2:c.302T>C	NP_001315986.1:p.Leu101Ser
NM_001329058.2:c.197+105T>C	NP_001315987.1:n.197+105T>C
NM_001382703.1:c.193+109T>C	NP_001369632.1:n.193+109T>C