Canonical Allele Identifier: CA475368267

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66278157C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66510686C>G , CM000673.2:g.66510686C>G	GRCh38
NC_000011.9:g.66278157C>G , CM000673.1:g.66278157C>G	GRCh37
NC_000011.8:g.66034733C>G	NCBI36
NG_009093.1:g.5039C>G
NG_032068.1:g.35278C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.27C>G MANE Select	ENSP00000317469.7:p.Ser9=
ENST00000318312.11:c.27C>G	ENSP00000317469.7:p.Ser9=
ENST00000393994.4:c.27C>G	ENSP00000377563.2:p.Ser9=
ENST00000419755.3:c.159-327C>G	ENSP00000398526.3:n.159-327C>G
ENST00000455748.6:c.27C>G	ENSP00000405764.2:p.Ser9=
ENST00000524907.5:n.17C>G
ENST00000525809.5:c.27C>G	ENSP00000431187.1:p.Ser9=
ENST00000526035.5:c.27C>G	ENSP00000434197.1:p.Ser9=
ENST00000526760.5:c.27C>G	ENSP00000432140.1:p.Ser9=
ENST00000526815.5:c.-370C>G	ENSP00000436860.1:n.-370C>G
ENST00000527251.5:c.-370C>G	ENSP00000434360.1:n.-370C>G
ENST00000529766.5:n.34C>G
ENST00000529955.5:n.45C>G
ENST00000532908.5:c.27C>G	ENSP00000431866.1:p.Ser9=
ENST00000533557.5:c.27C>G	ENSP00000434619.1:p.Ser9=
ENST00000533644.5:c.27C>G	ENSP00000436073.1:p.Ser9=
ENST00000534730.5:n.39C>G
ENST00000630659.2:c.27C>G	ENSP00000486455.1:p.Ser9=
NM_024649.4:c.27C>G	NP_078925.3:p.Ser9=
NM_024649.5:c.27C>G MANE Select	NP_078925.3:p.Ser9=