Canonical Allele Identifier: CA2499221197

Gene: BBS1

Linked Data

• ClinVar Variation Id: 1137174
• ClinVar RCV Id: RCV001473077
• dbSNP Id: rs2134771164

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514399C>T , CM000673.2:g.66514399C>T	GRCh38
NC_000011.9:g.66281870C>T , CM000673.1:g.66281870C>T	GRCh37
NC_000011.8:g.66038446C>T	NCBI36
NG_009093.1:g.8752C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.160-7C>T MANE Select	ENSP00000317469.7:n.160-7C>T
ENST00000318312.11:c.160-7C>T	ENSP00000317469.7:n.160-7C>T
ENST00000393994.4:c.160-7C>T	ENSP00000377563.2:n.160-7C>T
ENST00000419755.3:c.271-7C>T	ENSP00000398526.3:n.271-7C>T
ENST00000455748.6:c.160-7C>T	ENSP00000405764.2:n.160-7C>T
ENST00000524458.5:c.35-7C>T	ENSP00000436195.1:n.35-7C>T
ENST00000524705.2:c.-20-107C>T	ENSP00000436927.1:n.-20-107C>T
ENST00000524907.5:n.150-7C>T
ENST00000525809.5:c.160-1141C>T	ENSP00000431187.1:n.160-1141C>T
ENST00000526035.5:c.125-7C>T	ENSP00000434197.1:n.125-7C>T
ENST00000526760.5:c.125-7C>T	ENSP00000432140.1:n.125-7C>T
ENST00000526815.5:c.70-7C>T	ENSP00000436860.1:n.70-7C>T
ENST00000527251.5:c.35-7C>T	ENSP00000434360.1:n.35-7C>T
ENST00000529766.5:n.167-7C>T
ENST00000529955.5:n.178-7C>T
ENST00000532908.5:c.125-7C>T	ENSP00000431866.1:n.125-7C>T
ENST00000533557.5:c.125-7C>T	ENSP00000434619.1:n.125-7C>T
ENST00000533644.5:c.160-7C>T	ENSP00000436073.1:n.160-7C>T
ENST00000534730.5:n.172-7C>T
ENST00000630659.2:c.125-7C>T	ENSP00000486455.1:n.125-7C>T
NM_024649.4:c.160-7C>T	NP_078925.3:n.160-7C>T
NM_024649.5:c.160-7C>T MANE Select	NP_078925.3:n.160-7C>T