Canonical Allele Identifier: CA2047353122

Gene: BBS10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.76346026G= , CM000674.2:g.76346026G=	GRCh38
NC_000012.11:g.76739806G= , CM000674.1:g.76739806G=	GRCh37
NC_000012.10:g.75263937G=	NCBI36
NG_016357.1:g.7417C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650064.2:c.1959C= MANE Select	ENSP00000497413.1:p.Ser653=
ENST00000393262.3:c.1959C=	ENSP00000376946.3:p.Ser653=
NM_024685.3:c.1959C=	NP_078961.3:p.Ser653=
NM_024685.4:c.1959C= MANE Select	NP_078961.3:p.Ser653=