Canonical Allele Identifier: CA599874762

Gene: BBS1

Linked Data

• dbSNP Id: rs1401974639
• gnomAD v2: 11-66278195-C-T
• gnomAD v4: 11-66510724-C-T
• MyVariant Identifiers: chr11:g.66278195C>T (hg19) ; chr11:g.66510724C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66510724C>T , CM000673.2:g.66510724C>T	GRCh38
NC_000011.9:g.66278195C>T , CM000673.1:g.66278195C>T	GRCh37
NC_000011.8:g.66034771C>T	NCBI36
NG_009093.1:g.5077C>T
NG_032068.1:g.35316C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.47+18C>T MANE Select	ENSP00000317469.7:n.47+18C>T
ENST00000318312.11:c.47+18C>T	ENSP00000317469.7:n.47+18C>T
ENST00000393994.4:c.47+18C>T	ENSP00000377563.2:n.47+18C>T
ENST00000419755.3:c.159-289C>T	ENSP00000398526.3:n.159-289C>T
ENST00000455748.6:c.47+18C>T	ENSP00000405764.2:n.47+18C>T
ENST00000524907.5:n.37+18C>T
ENST00000525809.5:c.47+18C>T	ENSP00000431187.1:n.47+18C>T
ENST00000526035.5:c.47+18C>T	ENSP00000434197.1:n.47+18C>T
ENST00000526760.5:c.47+18C>T	ENSP00000432140.1:n.47+18C>T
ENST00000526815.5:c.-332C>T	ENSP00000436860.1:n.-332C>T
ENST00000527251.5:c.-332C>T	ENSP00000434360.1:n.-332C>T
ENST00000529766.5:n.54+18C>T
ENST00000529955.5:n.65+18C>T
ENST00000532908.5:c.47+18C>T	ENSP00000431866.1:n.47+18C>T
ENST00000533557.5:c.47+18C>T	ENSP00000434619.1:n.47+18C>T
ENST00000533644.5:c.47+18C>T	ENSP00000436073.1:n.47+18C>T
ENST00000534730.5:n.59+18C>T
ENST00000630659.2:c.47+18C>T	ENSP00000486455.1:n.47+18C>T
NM_024649.4:c.47+18C>T	NP_078925.3:n.47+18C>T
NM_024649.5:c.47+18C>T MANE Select	NP_078925.3:n.47+18C>T