Canonical Allele Identifier: CA385813877
Gene: BBS10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.76740902A>C (hg19) chr12:g.76347122A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347122A>C , CM000674.2:g.76347122A>C GRCh38
NC_000012.11:g.76740902A>C , CM000674.1:g.76740902A>C GRCh37
NC_000012.10:g.75265033A>C NCBI36
NG_016357.1:g.6321T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.863T>G MANE Select ENSP00000497413.1:p.Phe288Cys
ENST00000393262.3:c.863T>G ENSP00000376946.3:p.Phe288Cys
NM_024685.3:c.863T>G NP_078961.3:p.Phe288Cys
NM_024685.4:c.863T>G MANE Select NP_078961.3:p.Phe288Cys
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