Canonical Allele Identifier: CA385813772
Gene: BBS10 HGNC NCBI

Linked Data

dbSNP Id: rs1163017797
gnomAD v2: 12-76740876-T-C
gnomAD v4: 12-76347096-T-C
MyVariant Identifiers: chr12:g.76740876T>C (hg19) chr12:g.76347096T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347096T>C , CM000674.2:g.76347096T>C GRCh38
NC_000012.11:g.76740876T>C , CM000674.1:g.76740876T>C GRCh37
NC_000012.10:g.75265007T>C NCBI36
NG_016357.1:g.6347A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.889A>G MANE Select ENSP00000497413.1:p.Ile297Val
ENST00000393262.3:c.889A>G ENSP00000376946.3:p.Ile297Val
NM_024685.3:c.889A>G NP_078961.3:p.Ile297Val
NM_024685.4:c.889A>G MANE Select NP_078961.3:p.Ile297Val
Search 100 bp 5'
Search 100 bp 3'