Canonical Allele Identifier: CA2047353487
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346797A= , CM000674.2:g.76346797A= GRCh38
NC_000012.11:g.76740577A= , CM000674.1:g.76740577A= GRCh37
NC_000012.10:g.75264708A= NCBI36
NG_016357.1:g.6646T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.1188T= MANE Select ENSP00000497413.1:p.Ser396=
ENST00000393262.3:c.1188T= ENSP00000376946.3:p.Ser396=
NM_024685.3:c.1188T= NP_078961.3:p.Ser396=
NM_024685.4:c.1188T= MANE Select NP_078961.3:p.Ser396=