Canonical Allele Identifier: CA31391036

Gene: CRP

Linked Data

• dbSNP Id: rs868078724
• gnomAD v4: 1-159714533-G-A
• MyVariant Identifiers: chr1:g.159684323G>A (hg19) ; chr1:g.159714533G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714533G>A , CM000663.2:g.159714533G>A	GRCh38
NC_000001.10:g.159684323G>A , CM000663.1:g.159684323G>A	GRCh37
NC_000001.9:g.157950947G>A	NCBI36
NG_013007.1:g.5057C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.-48C>T MANE Select	ENSP00000255030.5:n.-48C>T
ENST00000368110.1:c.-48C>T	ENSP00000357091.1:n.-48C>T
ENST00000368111.5:c.-48C>T	ENSP00000357092.1:n.-48C>T
ENST00000368112.5:c.-48C>T	ENSP00000357093.1:n.-48C>T
ENST00000437342.1:c.-342C>T	ENSP00000402788.1:n.-342C>T
NM_000567.2:c.-48C>T	NP_000558.2:n.-48C>T
XM_011509207.1:c.-48C>T	XP_011507509.1:n.-48C>T
NM_001329057.1:c.-48C>T	NP_001315986.1:n.-48C>T
NM_001329058.1:c.-48C>T	NP_001315987.1:n.-48C>T
NM_000567.3:c.-48C>T MANE Select	NP_000558.2:n.-48C>T
NM_001329057.2:c.-48C>T	NP_001315986.1:n.-48C>T
NM_001329058.2:c.-48C>T	NP_001315987.1:n.-48C>T
NM_001382703.1:c.-48C>T	NP_001369632.1:n.-48C>T