Canonical Allele Identifier: CA31390089

Gene: CRP

Linked Data

• dbSNP Id: rs1025028306
• gnomAD v4: 1-159712455-A-G
• MyVariant Identifiers: chr1:g.159682245A>G (hg19) ; chr1:g.159712455A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712455A>G , CM000663.2:g.159712455A>G	GRCh38
NC_000001.10:g.159682245A>G , CM000663.1:g.159682245A>G	GRCh37
NC_000001.9:g.157948869A>G	NCBI36
NG_013007.1:g.7135T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1070T>C MANE Select	ENSP00000255030.5:n.*1070T>C
ENST00000368112.5:c.*362T>C	ENSP00000357093.1:n.*362T>C
ENST00000437342.1:c.*362T>C	ENSP00000402788.1:n.*362T>C
ENST00000473196.1:n.605T>C
NM_000567.2:c.*1070T>C	NP_000558.2:n.*1070T>C
XM_011509207.1:c.*362T>C	XP_011507509.1:n.*362T>C
NM_001329057.1:c.*362T>C	NP_001315986.1:n.*362T>C
NM_001329058.1:c.*136T>C	NP_001315987.1:n.*136T>C
NM_000567.3:c.*1070T>C MANE Select	NP_000558.2:n.*1070T>C
NM_001329057.2:c.*362T>C	NP_001315986.1:n.*362T>C
NM_001329058.2:c.*136T>C	NP_001315987.1:n.*136T>C
NM_001382703.1:c.*1070T>C	NP_001369632.1:n.*1070T>C