Canonical Allele Identifier: CA385813649
Gene: BBS10 HGNC NCBI

Linked Data

dbSNP Id: rs1565809903
gnomAD v2: 12-76740852-T-C
gnomAD v4: 12-76347072-T-C
MyVariant Identifiers: chr12:g.76740852T>C (hg19) chr12:g.76740852_76740856delinsCCTGA (hg19) chr12:g.76347072T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347072T>C , CM000674.2:g.76347072T>C GRCh38
NC_000012.11:g.76740852T>C , CM000674.1:g.76740852T>C GRCh37
NC_000012.10:g.75264983T>C NCBI36
NG_016357.1:g.6371A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.913A>G MANE Select ENSP00000497413.1:p.Asn305Asp
ENST00000393262.3:c.913A>G ENSP00000376946.3:p.Asn305Asp
NM_024685.3:c.913A>G NP_078961.3:p.Asn305Asp
NM_024685.4:c.913A>G MANE Select NP_078961.3:p.Asn305Asp
Search 100 bp 5'
Search 100 bp 3'