Canonical Allele Identifier: CA1189284
Gene: CRP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1417938

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159714396T>A , CM000663.2:g.159714396T>A GRCh38
NC_000001.10:g.159684186T>A , CM000663.1:g.159684186T>A GRCh37
NC_000001.9:g.157950810T>A NCBI36
NG_013007.1:g.5194A>T

Transcript Alleles

HGVS Amino-acid change
NM_000567.2:c.61+29A>T VV NP_000558.2:p.=
XM_011509207.1:c.61+29A>T XP_011507509.1:p.=
NM_001329057.1:c.61+29A>T VV NP_001315986.1:p.=
NM_001329058.1:c.61+29A>T VV NP_001315987.1:p.=
NM_000567.3:c.61+29A>T VV MANE Preferred NP_000558.2:p.=
ENST00000255030.9:c.61+29A>T ENSP00000255030.5:p.=
ENST00000368110.1:c.61+29A>T ENSP00000357091.1:p.=
ENST00000368111.5:c.61+29A>T ENSP00000357092.1:p.=
ENST00000368112.5:c.61+29A>T ENSP00000357093.1:p.=
ENST00000437342.1:c.-308+103A>T ENSP00000402788.1:p.=