Canonical Allele Identifier: CA2047353004
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345733A= , CM000674.2:g.76345733A= GRCh38
NC_000012.11:g.76739513A= , CM000674.1:g.76739513A= GRCh37
NC_000012.10:g.75263644A= NCBI36
NG_016357.1:g.7710T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.*80T= MANE Select ENSP00000497413.1:n.*80T=
ENST00000393262.3:c.*80T= ENSP00000376946.3:n.*80T=
NM_024685.3:c.*80T= NP_078961.3:n.*80T=
NM_024685.4:c.*80T= MANE Select NP_078961.3:n.*80T=