Canonical Allele Identifier: CA481011451
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2862122
ClinVar RCV Id: RCV003633039
MyVariant Identifiers: chr12:g.76740922T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347142T>G , CM000674.2:g.76347142T>G GRCh38
NC_000012.11:g.76740922T>G , CM000674.1:g.76740922T>G GRCh37
NC_000012.10:g.75265053T>G NCBI36
NG_016357.1:g.6301A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.843A>C MANE Select ENSP00000497413.1:p.Ala281=
ENST00000393262.3:c.843A>C ENSP00000376946.3:p.Ala281=
NM_024685.3:c.843A>C NP_078961.3:p.Ala281=
NM_024685.4:c.843A>C MANE Select NP_078961.3:p.Ala281=
Search 100 bp 5'
Search 100 bp 3'