Canonical Allele Identifier: CA385813882
Gene: BBS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347123A>T , CM000674.2:g.76347123A>T GRCh38
NC_000012.11:g.76740903A>T , CM000674.1:g.76740903A>T GRCh37
NC_000012.10:g.75265034A>T NCBI36
NG_016357.1:g.6320T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.862T>A MANE Select ENSP00000497413.1:p.Phe288Ile
ENST00000393262.3:c.862T>A ENSP00000376946.3:p.Phe288Ile
NM_024685.3:c.862T>A NP_078961.3:p.Phe288Ile
NM_024685.4:c.862T>A MANE Select NP_078961.3:p.Phe288Ile