Canonical Allele Identifier: CA385815447
Gene: BBS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76347625C>G , CM000674.2:g.76347625C>G GRCh38
NC_000012.11:g.76741405C>G , CM000674.1:g.76741405C>G GRCh37
NC_000012.10:g.75265536C>G NCBI36
NG_016357.1:g.5818G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.360G>C MANE Select ENSP00000497413.1:p.Trp120Cys
ENST00000393262.3:c.360G>C ENSP00000376946.3:p.Trp120Cys
NM_024685.3:c.360G>C NP_078961.3:p.Trp120Cys
NM_024685.4:c.360G>C MANE Select NP_078961.3:p.Trp120Cys