Canonical Allele Identifier: CA2047353600

Gene: BBS10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.76347030C= , CM000674.2:g.76347030C=	GRCh38
NC_000012.11:g.76740810C= , CM000674.1:g.76740810C=	GRCh37
NC_000012.10:g.75264941C=	NCBI36
NG_016357.1:g.6413G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650064.2:c.955G= MANE Select	ENSP00000497413.1:p.Val319=
ENST00000393262.3:c.955G=	ENSP00000376946.3:p.Val319=
NM_024685.3:c.955G=	NP_078961.3:p.Val319=
NM_024685.4:c.955G= MANE Select	NP_078961.3:p.Val319=