Canonical Allele Identifier: CA2047353020
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345769G= , CM000674.2:g.76345769G= GRCh38
NC_000012.11:g.76739549G= , CM000674.1:g.76739549G= GRCh37
NC_000012.10:g.75263680G= NCBI36
NG_016357.1:g.7674C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.*44C= MANE Select ENSP00000497413.1:n.*44C=
ENST00000393262.3:c.*44C= ENSP00000376946.3:n.*44C=
NM_024685.3:c.*44C= NP_078961.3:n.*44C=
NM_024685.4:c.*44C= MANE Select NP_078961.3:n.*44C=