Canonical Allele Identifier: CA31390661

Gene: CRP

Linked Data

• dbSNP Id: rs34340208
• gnomAD v2: 1-159683493-C-T
• gnomAD v3: 1-159713703-C-T
• gnomAD v4: 1-159713703-C-T
• MyVariant Identifiers: chr1:g.159683493C>T (hg19) ; chr1:g.159713703C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713703C>T , CM000663.2:g.159713703C>T	GRCh38
NC_000001.10:g.159683493C>T , CM000663.1:g.159683493C>T	GRCh37
NC_000001.9:g.157950117C>T	NCBI36
NG_013007.1:g.5887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.497G>A MANE Select	ENSP00000255030.5:p.Gly166Glu
ENST00000368110.1:c.194-63G>A	ENSP00000357091.1:n.194-63G>A
ENST00000368111.5:c.194-63G>A	ENSP00000357092.1:n.194-63G>A
ENST00000368112.5:c.198-100G>A	ENSP00000357093.1:n.198-100G>A
ENST00000437342.1:c.-38G>A	ENSP00000402788.1:n.-38G>A
ENST00000473196.1:n.65G>A
ENST00000489317.1:n.74+304G>A
NM_000567.2:c.497G>A	NP_000558.2:p.Gly166Glu
XM_011509207.1:c.497G>A	XP_011507509.1:p.Gly166Glu
NM_001329057.1:c.497G>A	NP_001315986.1:p.Gly166Glu
NM_001329058.1:c.198-100G>A	NP_001315987.1:n.198-100G>A
NM_000567.3:c.497G>A MANE Select	NP_000558.2:p.Gly166Glu
NM_001329057.2:c.497G>A	NP_001315986.1:p.Gly166Glu
NM_001329058.2:c.198-100G>A	NP_001315987.1:n.198-100G>A
NM_001382703.1:c.194-63G>A	NP_001369632.1:n.194-63G>A