Canonical Allele Identifier: CA481010572
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 990672
ClinVar RCV Id: RCV001278737
dbSNP Id: rs1951752945
gnomAD v4: 12-76345828-T-C
MyVariant Identifiers: chr12:g.76739608T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345828T>C , CM000674.2:g.76345828T>C GRCh38
NC_000012.11:g.76739608T>C , CM000674.1:g.76739608T>C GRCh37
NC_000012.10:g.75263739T>C NCBI36
NG_016357.1:g.7615A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.2157A>G MANE Select ENSP00000497413.1:p.Ser719=
ENST00000393262.3:c.2157A>G ENSP00000376946.3:p.Ser719=
NM_024685.3:c.2157A>G NP_078961.3:p.Ser719=
NM_024685.4:c.2157A>G MANE Select NP_078961.3:p.Ser719=
Search 100 bp 5'
Search 100 bp 3'