Canonical Allele Identifier: CA2047353630
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347126G= , CM000674.2:g.76347126G= GRCh38
NC_000012.11:g.76740906G= , CM000674.1:g.76740906G= GRCh37
NC_000012.10:g.75265037G= NCBI36
NG_016357.1:g.6317C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.859C= MANE Select ENSP00000497413.1:p.Gln287=
ENST00000393262.3:c.859C= ENSP00000376946.3:p.Gln287=
NM_024685.3:c.859C= NP_078961.3:p.Gln287=
NM_024685.4:c.859C= MANE Select NP_078961.3:p.Gln287=