Canonical Allele Identifier: CA349161418
Gene: BBS5 HGNC NCBI

Linked Data

dbSNP Id: rs1338148111

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487822C>A , CM000664.2:g.169487822C>A GRCh38
NC_000002.11:g.170344332C>A , CM000664.1:g.170344332C>A GRCh37
NC_000002.10:g.170052578C>A NCBI36
NG_011567.1:g.13327C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.225C>A MANE Select ENSP00000295240.3:p.Cys75Ter
ENST00000295240.7:c.225C>A ENSP00000295240.3:p.Cys75Ter
ENST00000392663.6:c.225C>A ENSP00000376431.2:p.Cys75Ter
ENST00000443151.1:c.143-165C>A ENSP00000406182.1:n.143-165C>A
ENST00000475571.1:n.61C>A
ENST00000513963.1:c.225C>A ENSP00000424363.1:p.Cys75Ter
NM_152384.2:c.225C>A NP_689597.1:p.Cys75Ter
NM_152384.3:c.225C>A MANE Select NP_689597.1:p.Cys75Ter