Canonical Allele Identifier: CA481011150
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2728497
ClinVar RCV Id: RCV003524961
dbSNP Id: rs1951756955
MyVariant Identifiers: chr12:g.76740061A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346281A>G , CM000674.2:g.76346281A>G GRCh38
NC_000012.11:g.76740061A>G , CM000674.1:g.76740061A>G GRCh37
NC_000012.10:g.75264192A>G NCBI36
NG_016357.1:g.7162T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1704T>C MANE Select ENSP00000497413.1:p.Thr568=
ENST00000393262.3:c.1704T>C ENSP00000376946.3:p.Thr568=
NM_024685.3:c.1704T>C NP_078961.3:p.Thr568=
NM_024685.4:c.1704T>C MANE Select NP_078961.3:p.Thr568=
Search 100 bp 5'
Search 100 bp 3'