Canonical Allele Identifier: CA2047353263
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346345G= , CM000674.2:g.76346345G= GRCh38
NC_000012.11:g.76740125G= , CM000674.1:g.76740125G= GRCh37
NC_000012.10:g.75264256G= NCBI36
NG_016357.1:g.7098C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.1640C= MANE Select ENSP00000497413.1:p.Ala547=
ENST00000393262.3:c.1640C= ENSP00000376946.3:p.Ala547=
NM_024685.3:c.1640C= NP_078961.3:p.Ala547=
NM_024685.4:c.1640C= MANE Select NP_078961.3:p.Ala547=