Canonical Allele Identifier: CA31390295

Gene: CRP

Linked Data

• dbSNP Id: rs760110048
• gnomAD v2: 1-159682643-T-A
• gnomAD v3: 1-159712853-T-A
• gnomAD v4: 1-159712853-T-A
• MyVariant Identifiers: chr1:g.159682643T>A (hg19) ; chr1:g.159712853T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712853T>A , CM000663.2:g.159712853T>A	GRCh38
NC_000001.10:g.159682643T>A , CM000663.1:g.159682643T>A	GRCh37
NC_000001.9:g.157949267T>A	NCBI36
NG_013007.1:g.6737A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*672A>T MANE Select	ENSP00000255030.5:n.*672A>T
ENST00000368110.1:c.*23-59A>T	ENSP00000357091.1:n.*23-59A>T
ENST00000368111.5:c.*23-273A>T	ENSP00000357092.1:n.*23-273A>T
ENST00000368112.5:c.*23-59A>T	ENSP00000357093.1:n.*23-59A>T
ENST00000437342.1:c.*23-59A>T	ENSP00000402788.1:n.*23-59A>T
ENST00000473196.1:n.266-59A>T
ENST00000489317.1:n.75-59A>T
NM_000567.2:c.*672A>T	NP_000558.2:n.*672A>T
XM_011509207.1:c.*23-59A>T	XP_011507509.1:n.*23-59A>T
NM_001329057.1:c.*23-59A>T	NP_001315986.1:n.*23-59A>T
NM_001329058.1:c.*23-285A>T	NP_001315987.1:n.*23-285A>T
NM_000567.3:c.*672A>T MANE Select	NP_000558.2:n.*672A>T
NM_001329057.2:c.*23-59A>T	NP_001315986.1:n.*23-59A>T
NM_001329058.2:c.*23-285A>T	NP_001315987.1:n.*23-285A>T
NM_001382703.1:c.*672A>T	NP_001369632.1:n.*672A>T