Canonical Allele Identifier: CA481011287
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1993633
ClinVar RCV Id: RCV002801548
MyVariant Identifiers: chr12:g.76740382A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346602A>T , CM000674.2:g.76346602A>T GRCh38
NC_000012.11:g.76740382A>T , CM000674.1:g.76740382A>T GRCh37
NC_000012.10:g.75264513A>T NCBI36
NG_016357.1:g.6841T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1383T>A MANE Select ENSP00000497413.1:p.Gly461=
ENST00000393262.3:c.1383T>A ENSP00000376946.3:p.Gly461=
NM_024685.3:c.1383T>A NP_078961.3:p.Gly461=
NM_024685.4:c.1383T>A MANE Select NP_078961.3:p.Gly461=
Search 100 bp 5'
Search 100 bp 3'