Canonical Allele Identifier: CA1189203
Gene: CRP HGNC NCBI

Linked Data

dbSNP Id: rs771088315

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713871G>A , CM000663.2:g.159713871G>A GRCh38
NC_000001.10:g.159683661G>A , CM000663.1:g.159683661G>A GRCh37
NC_000001.9:g.157950285G>A NCBI36
NG_013007.1:g.5719C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.329C>T MANE Select ENSP00000255030.5:p.Ala110Val
ENST00000368110.1:c.193+136C>T ENSP00000357091.1:n.193+136C>T
ENST00000368111.5:c.193+136C>T ENSP00000357092.1:n.193+136C>T
ENST00000368112.5:c.197+132C>T ENSP00000357093.1:n.197+132C>T
ENST00000437342.1:c.-206C>T ENSP00000402788.1:n.-206C>T
ENST00000489317.1:n.74+136C>T
NM_000567.2:c.329C>T NP_000558.2:p.Ala110Val
XM_011509207.1:c.329C>T XP_011507509.1:p.Ala110Val
NM_001329057.1:c.329C>T NP_001315986.1:p.Ala110Val
NM_001329058.1:c.197+132C>T NP_001315987.1:n.197+132C>T
NM_000567.3:c.329C>T MANE Select NP_000558.2:p.Ala110Val
NM_001329057.2:c.329C>T NP_001315986.1:p.Ala110Val
NM_001329058.2:c.197+132C>T NP_001315987.1:n.197+132C>T
NM_001382703.1:c.193+136C>T NP_001369632.1:n.193+136C>T