Canonical Allele Identifier: CA385815698
Gene: BBS10 HGNC NCBI

Linked Data

dbSNP Id: rs2136091216

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347637A>C , CM000674.2:g.76347637A>C GRCh38
NC_000012.11:g.76741417A>C , CM000674.1:g.76741417A>C GRCh37
NC_000012.10:g.75265548A>C NCBI36
NG_016357.1:g.5806T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.348T>G MANE Select ENSP00000497413.1:p.His116Gln
ENST00000393262.3:c.348T>G ENSP00000376946.3:p.His116Gln
NM_024685.3:c.348T>G NP_078961.3:p.His116Gln
NM_024685.4:c.348T>G MANE Select NP_078961.3:p.His116Gln