Canonical Allele Identifier: CA2047353638

Gene: BBS10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.76347144C= , CM000674.2:g.76347144C=	GRCh38
NC_000012.11:g.76740924C= , CM000674.1:g.76740924C=	GRCh37
NC_000012.10:g.75265055C=	NCBI36
NG_016357.1:g.6299G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650064.2:c.841G= MANE Select	ENSP00000497413.1:p.Ala281=
ENST00000393262.3:c.841G=	ENSP00000376946.3:p.Ala281=
NM_024685.3:c.841G=	NP_078961.3:p.Ala281=
NM_024685.4:c.841G= MANE Select	NP_078961.3:p.Ala281=