Canonical Allele Identifier: CA6694128
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 434483
ClinVar RCV Id: RCV000504274
dbSNP Id: rs769632511
ExAC: 12:76740091 A / C
gnomAD v2: 12-76740091-A-C
gnomAD v4: 12-76346311-A-C
MyVariant Identifiers: chr12:g.76740091A>C (hg19) chr12:g.76346311A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346311A>C , CM000674.2:g.76346311A>C GRCh38
NC_000012.11:g.76740091A>C , CM000674.1:g.76740091A>C GRCh37
NC_000012.10:g.75264222A>C NCBI36
NG_016357.1:g.7132T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1674T>G MANE Select ENSP00000497413.1:p.Ser558=
ENST00000393262.3:c.1674T>G ENSP00000376946.3:p.Ser558=
NM_024685.3:c.1674T>G NP_078961.3:p.Ser558=
NM_024685.4:c.1674T>G MANE Select NP_078961.3:p.Ser558=
Search 100 bp 5'
Search 100 bp 3'