Canonical Allele Identifier: CA1979718810
Gene: BBS1 HGNC NCBI

Linked Data

dbSNP Id: rs1764977301

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515778G>A , CM000673.2:g.66515778G>A GRCh38
NC_000011.9:g.66283249G>A , CM000673.1:g.66283249G>A GRCh37
NC_000011.8:g.66039825G>A NCBI36
NG_009093.1:g.10131G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.518+47G>A MANE Select ENSP00000317469.7:n.518+47G>A
ENST00000318312.11:c.518+47G>A ENSP00000317469.7:n.518+47G>A
ENST00000393994.4:c.518+47G>A ENSP00000377563.2:n.518+47G>A
ENST00000419755.3:c.629+47G>A ENSP00000398526.3:n.629+47G>A
ENST00000455748.6:c.432+1100G>A ENSP00000405764.2:n.432+1100G>A
ENST00000524458.5:c.*225G>A ENSP00000436195.1:n.*225G>A
ENST00000524907.5:n.614+47G>A
ENST00000525809.5:c.245+47G>A ENSP00000431187.1:n.245+47G>A
ENST00000526035.5:c.*225+47G>A ENSP00000434197.1:n.*225+47G>A
ENST00000526760.5:c.*225+47G>A ENSP00000432140.1:n.*225+47G>A
ENST00000527251.5:c.*225+47G>A ENSP00000434360.1:n.*225+47G>A
ENST00000528543.1:n.40+47G>A
ENST00000529766.5:n.525+47G>A
ENST00000529953.5:n.170+47G>A
ENST00000529955.5:n.489+47G>A
ENST00000532908.5:c.*178+47G>A ENSP00000431866.1:n.*178+47G>A
ENST00000533430.5:n.296+47G>A
ENST00000533557.5:c.*178+47G>A ENSP00000434619.1:n.*178+47G>A
ENST00000533644.5:c.471+47G>A ENSP00000436073.1:n.471+47G>A
ENST00000534730.5:n.577G>A
ENST00000630659.2:c.*225+47G>A ENSP00000486455.1:n.*225+47G>A
NM_024649.4:c.518+47G>A NP_078925.3:n.518+47G>A
NM_024649.5:c.518+47G>A MANE Select NP_078925.3:n.518+47G>A