Canonical Allele Identifier: CA385813898
Gene: BBS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347132T>A , CM000674.2:g.76347132T>A GRCh38
NC_000012.11:g.76740912T>A , CM000674.1:g.76740912T>A GRCh37
NC_000012.10:g.75265043T>A NCBI36
NG_016357.1:g.6311A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.853A>T MANE Select ENSP00000497413.1:p.Thr285Ser
ENST00000393262.3:c.853A>T ENSP00000376946.3:p.Thr285Ser
NM_024685.3:c.853A>T NP_078961.3:p.Thr285Ser
NM_024685.4:c.853A>T MANE Select NP_078961.3:p.Thr285Ser