Canonical Allele Identifier: CA385812402
Gene: BBS10 HGNC NCBI

Linked Data

dbSNP Id: rs867485840

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346798G>C , CM000674.2:g.76346798G>C GRCh38
NC_000012.11:g.76740578G>C , CM000674.1:g.76740578G>C GRCh37
NC_000012.10:g.75264709G>C NCBI36
NG_016357.1:g.6645C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.1187C>G MANE Select ENSP00000497413.1:p.Ser396Cys
ENST00000393262.3:c.1187C>G ENSP00000376946.3:p.Ser396Cys
NM_024685.3:c.1187C>G NP_078961.3:p.Ser396Cys
NM_024685.4:c.1187C>G MANE Select NP_078961.3:p.Ser396Cys