Canonical Allele Identifier: CA1979718842
Gene: BBS1 HGNC NCBI

Linked Data

dbSNP Id: rs1856037646

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515800A>G , CM000673.2:g.66515800A>G GRCh38
NC_000011.9:g.66283271A>G , CM000673.1:g.66283271A>G GRCh37
NC_000011.8:g.66039847A>G NCBI36
NG_009093.1:g.10153A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.519-61A>G MANE Select ENSP00000317469.7:n.519-61A>G
ENST00000318312.11:c.519-61A>G ENSP00000317469.7:n.519-61A>G
ENST00000393994.4:c.519-61A>G ENSP00000377563.2:n.519-61A>G
ENST00000419755.3:c.630-61A>G ENSP00000398526.3:n.630-61A>G
ENST00000455748.6:c.432+1122A>G ENSP00000405764.2:n.432+1122A>G
ENST00000524458.5:c.*247A>G ENSP00000436195.1:n.*247A>G
ENST00000524907.5:n.615-61A>G
ENST00000525809.5:c.246-61A>G ENSP00000431187.1:n.246-61A>G
ENST00000526035.5:c.*226-61A>G ENSP00000434197.1:n.*226-61A>G
ENST00000526760.5:c.*226-61A>G ENSP00000432140.1:n.*226-61A>G
ENST00000527251.5:c.*226-61A>G ENSP00000434360.1:n.*226-61A>G
ENST00000528543.1:n.41-61A>G
ENST00000529766.5:n.526-61A>G
ENST00000529953.5:n.171-61A>G
ENST00000529955.5:n.490-61A>G
ENST00000532908.5:c.*179-61A>G ENSP00000431866.1:n.*179-61A>G
ENST00000533430.5:n.297-61A>G
ENST00000533557.5:c.*179-61A>G ENSP00000434619.1:n.*179-61A>G
ENST00000533644.5:c.472-61A>G ENSP00000436073.1:n.472-61A>G
ENST00000534730.5:n.599A>G
ENST00000630659.2:c.*226-61A>G ENSP00000486455.1:n.*226-61A>G
NM_024649.4:c.519-61A>G NP_078925.3:n.519-61A>G
NM_024649.5:c.519-61A>G MANE Select NP_078925.3:n.519-61A>G