Canonical Allele Identifier: CA1189153

Gene: CRP

Linked Data

• dbSNP Id: rs754981672
• ExAC: 1:159683426 C / T
• gnomAD v2: 1-159683426-C-T
• gnomAD v4: 1-159713636-C-T
• MyVariant Identifiers: chr1:g.159683426C>T (hg19) ; chr1:g.159713636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713636C>T , CM000663.2:g.159713636C>T	GRCh38
NC_000001.10:g.159683426C>T , CM000663.1:g.159683426C>T	GRCh37
NC_000001.9:g.157950050C>T	NCBI36
NG_013007.1:g.5954G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.564G>A MANE Select	ENSP00000255030.5:p.Glu188=
ENST00000368110.1:c.198G>A	ENSP00000357091.1:p.Glu66=
ENST00000368111.5:c.198G>A	ENSP00000357092.1:p.Glu66=
ENST00000368112.5:c.198-33G>A	ENSP00000357093.1:n.198-33G>A
ENST00000437342.1:c.30G>A	ENSP00000402788.1:p.Glu10=
ENST00000473196.1:n.132G>A
ENST00000489317.1:n.74+371G>A
NM_000567.2:c.564G>A	NP_000558.2:p.Glu188=
XM_011509207.1:c.564G>A	XP_011507509.1:p.Glu188=
NM_001329057.1:c.564G>A	NP_001315986.1:p.Glu188=
NM_001329058.1:c.198-33G>A	NP_001315987.1:n.198-33G>A
NM_000567.3:c.564G>A MANE Select	NP_000558.2:p.Glu188=
NM_001329057.2:c.564G>A	NP_001315986.1:p.Glu188=
NM_001329058.2:c.198-33G>A	NP_001315987.1:n.198-33G>A
NM_001382703.1:c.198G>A	NP_001369632.1:p.Glu66=