Canonical Allele Identifier: CA385813915
Gene: BBS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347139C>A , CM000674.2:g.76347139C>A GRCh38
NC_000012.11:g.76740919C>A , CM000674.1:g.76740919C>A GRCh37
NC_000012.10:g.75265050C>A NCBI36
NG_016357.1:g.6304G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.846G>T MANE Select ENSP00000497413.1:p.Gln282His
ENST00000393262.3:c.846G>T ENSP00000376946.3:p.Gln282His
NM_024685.3:c.846G>T NP_078961.3:p.Gln282His
NM_024685.4:c.846G>T MANE Select NP_078961.3:p.Gln282His