Canonical Allele Identifier: CA385813913
Gene: BBS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347138A>G , CM000674.2:g.76347138A>G GRCh38
NC_000012.11:g.76740918A>G , CM000674.1:g.76740918A>G GRCh37
NC_000012.10:g.75265049A>G NCBI36
NG_016357.1:g.6305T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.847T>C MANE Select ENSP00000497413.1:p.Phe283Leu
ENST00000393262.3:c.847T>C ENSP00000376946.3:p.Phe283Leu
NM_024685.3:c.847T>C NP_078961.3:p.Phe283Leu
NM_024685.4:c.847T>C MANE Select NP_078961.3:p.Phe283Leu