Canonical Allele Identifier: CA6694100
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1157037
ClinVar RCV Id: RCV001499925
dbSNP Id: rs753129922
ExAC: 12:76739941 G / A
gnomAD v2: 12-76739941-G-A
MyVariant Identifiers: chr12:g.76739941G>A (hg19) chr12:g.76346161G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346161G>A , CM000674.2:g.76346161G>A GRCh38
NC_000012.11:g.76739941G>A , CM000674.1:g.76739941G>A GRCh37
NC_000012.10:g.75264072G>A NCBI36
NG_016357.1:g.7282C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1824C>T MANE Select ENSP00000497413.1:p.Ile608=
ENST00000393262.3:c.1824C>T ENSP00000376946.3:p.Ile608=
NM_024685.3:c.1824C>T NP_078961.3:p.Ile608=
NM_024685.4:c.1824C>T MANE Select NP_078961.3:p.Ile608=
Search 100 bp 5'
Search 100 bp 3'