Canonical Allele Identifier: CA481011169
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2881985
ClinVar RCV Id: RCV003633280
MyVariant Identifiers: chr12:g.76740067A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346287A>G , CM000674.2:g.76346287A>G GRCh38
NC_000012.11:g.76740067A>G , CM000674.1:g.76740067A>G GRCh37
NC_000012.10:g.75264198A>G NCBI36
NG_016357.1:g.7156T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1698T>C MANE Select ENSP00000497413.1:p.Asn566=
ENST00000393262.3:c.1698T>C ENSP00000376946.3:p.Asn566=
NM_024685.3:c.1698T>C NP_078961.3:p.Asn566=
NM_024685.4:c.1698T>C MANE Select NP_078961.3:p.Asn566=
Search 100 bp 5'
Search 100 bp 3'