Canonical Allele Identifier: CA16041584
Gene: BBS10 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370877
dbSNP Id: rs1057516836

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347128_76347129dup , CM000674.2:g.76347128_76347129dup GRCh38
NC_000012.11:g.76740908_76740909dup , CM000674.1:g.76740908_76740909dup GRCh37
NC_000012.10:g.75265039_75265040dup NCBI36
NG_016357.1:g.6316_6317dup

Transcript Alleles

HGVS Amino-acid change
NM_024685.3:c.858_859dup VV
NM_024685.4:c.858_859dup VV
ENST00000393262.3:c.858_859dup