Canonical Allele Identifier: CA31390049

Gene: CRP

Linked Data

• dbSNP Id: rs979136086
• gnomAD v3: 1-159712361-G-A
• gnomAD v4: 1-159712361-G-A
• MyVariant Identifiers: chr1:g.159682151G>A (hg19) ; chr1:g.159712361G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712361G>A , CM000663.2:g.159712361G>A	GRCh38
NC_000001.10:g.159682151G>A , CM000663.1:g.159682151G>A	GRCh37
NC_000001.9:g.157948775G>A	NCBI36
NG_013007.1:g.7229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1164C>T MANE Select	ENSP00000255030.5:n.*1164C>T
ENST00000437342.1:c.*456C>T	ENSP00000402788.1:n.*456C>T
ENST00000473196.1:n.699C>T
NM_000567.2:c.*1164C>T	NP_000558.2:n.*1164C>T
XM_011509207.1:c.*456C>T	XP_011507509.1:n.*456C>T
NM_001329057.1:c.*456C>T	NP_001315986.1:n.*456C>T
NM_001329058.1:c.*230C>T	NP_001315987.1:n.*230C>T
NM_000567.3:c.*1164C>T MANE Select	NP_000558.2:n.*1164C>T
NM_001329057.2:c.*456C>T	NP_001315986.1:n.*456C>T
NM_001329058.2:c.*230C>T	NP_001315987.1:n.*230C>T
NM_001382703.1:c.*1164C>T	NP_001369632.1:n.*1164C>T