Canonical Allele Identifier: CA1979718905
Gene: BBS1 HGNC NCBI

Linked Data

dbSNP Id: rs1856038519

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515850T>A , CM000673.2:g.66515850T>A GRCh38
NC_000011.9:g.66283321T>A , CM000673.1:g.66283321T>A GRCh37
NC_000011.8:g.66039897T>A NCBI36
NG_009093.1:g.10203T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.519-11T>A MANE Select ENSP00000317469.7:n.519-11T>A
ENST00000318312.11:c.519-11T>A ENSP00000317469.7:n.519-11T>A
ENST00000393994.4:c.519-11T>A ENSP00000377563.2:n.519-11T>A
ENST00000419755.3:c.630-11T>A ENSP00000398526.3:n.630-11T>A
ENST00000455748.6:c.432+1172T>A ENSP00000405764.2:n.432+1172T>A
ENST00000524458.5:c.*297T>A ENSP00000436195.1:n.*297T>A
ENST00000524907.5:n.615-11T>A
ENST00000525809.5:c.246-11T>A ENSP00000431187.1:n.246-11T>A
ENST00000526035.5:c.*226-11T>A ENSP00000434197.1:n.*226-11T>A
ENST00000526760.5:c.*226-11T>A ENSP00000432140.1:n.*226-11T>A
ENST00000527251.5:c.*226-11T>A ENSP00000434360.1:n.*226-11T>A
ENST00000528543.1:n.41-11T>A
ENST00000529766.5:n.526-11T>A
ENST00000529953.5:n.171-11T>A
ENST00000529955.5:n.490-11T>A
ENST00000532908.5:c.*179-11T>A ENSP00000431866.1:n.*179-11T>A
ENST00000533430.5:n.297-11T>A
ENST00000533557.5:c.*179-11T>A ENSP00000434619.1:n.*179-11T>A
ENST00000533644.5:c.472-11T>A ENSP00000436073.1:n.472-11T>A
ENST00000630659.2:c.*226-11T>A ENSP00000486455.1:n.*226-11T>A
NM_024649.4:c.519-11T>A NP_078925.3:n.519-11T>A
NM_024649.5:c.519-11T>A MANE Select NP_078925.3:n.519-11T>A