Canonical Allele Identifier: CA2047353128

Gene: BBS10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.76346035T= , CM000674.2:g.76346035T=	GRCh38
NC_000012.11:g.76739815T= , CM000674.1:g.76739815T=	GRCh37
NC_000012.10:g.75263946T=	NCBI36
NG_016357.1:g.7408A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650064.2:c.1950A= MANE Select	ENSP00000497413.1:p.Gly650=
ENST00000393262.3:c.1950A=	ENSP00000376946.3:p.Gly650=
NM_024685.3:c.1950A=	NP_078961.3:p.Gly650=
NM_024685.4:c.1950A= MANE Select	NP_078961.3:p.Gly650=