Canonical Allele Identifier: CA2047353019
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345768G= , CM000674.2:g.76345768G= GRCh38
NC_000012.11:g.76739548G= , CM000674.1:g.76739548G= GRCh37
NC_000012.10:g.75263679G= NCBI36
NG_016357.1:g.7675C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.*45C= MANE Select ENSP00000497413.1:n.*45C=
ENST00000393262.3:c.*45C= ENSP00000376946.3:n.*45C=
NM_024685.3:c.*45C= NP_078961.3:n.*45C=
NM_024685.4:c.*45C= MANE Select NP_078961.3:n.*45C=