Canonical Allele Identifier: CA385809910
Gene: BBS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346199C>A , CM000674.2:g.76346199C>A GRCh38
NC_000012.11:g.76739979C>A , CM000674.1:g.76739979C>A GRCh37
NC_000012.10:g.75264110C>A NCBI36
NG_016357.1:g.7244G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1786G>T MANE Select ENSP00000497413.1:p.Ala596Ser
ENST00000393262.3:c.1786G>T ENSP00000376946.3:p.Ala596Ser
NM_024685.3:c.1786G>T NP_078961.3:p.Ala596Ser
NM_024685.4:c.1786G>T MANE Select NP_078961.3:p.Ala596Ser