Canonical Allele Identifier: CA385810745
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1471349
ClinVar RCV Id: RCV002002623
dbSNP Id: rs1444034224
gnomAD v2: 12-76740137-T-C
gnomAD v3: 12-76346357-T-C
gnomAD v4: 12-76346357-T-C
COSMIC: COSM1184499
MyVariant Identifiers: chr12:g.76740137T>C (hg19) chr12:g.76346357T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346357T>C , CM000674.2:g.76346357T>C GRCh38
NC_000012.11:g.76740137T>C , CM000674.1:g.76740137T>C GRCh37
NC_000012.10:g.75264268T>C NCBI36
NG_016357.1:g.7086A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1628A>G MANE Select ENSP00000497413.1:p.Asn543Ser
ENST00000393262.3:c.1628A>G ENSP00000376946.3:p.Asn543Ser
NM_024685.3:c.1628A>G NP_078961.3:p.Asn543Ser
NM_024685.4:c.1628A>G MANE Select NP_078961.3:p.Asn543Ser
Search 100 bp 5'
Search 100 bp 3'