Canonical Allele Identifier: CA2619945558
Gene: BBS10 HGNC NCBI

Linked Data

gnomAD v4: 12-76345754-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345754T>A , CM000674.2:g.76345754T>A GRCh38
NC_000012.11:g.76739534T>A , CM000674.1:g.76739534T>A GRCh37
NC_000012.10:g.75263665T>A NCBI36
NG_016357.1:g.7689A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.*59A>T MANE Select ENSP00000497413.1:n.*59A>T
ENST00000393262.3:c.*59A>T ENSP00000376946.3:n.*59A>T
NM_024685.3:c.*59A>T NP_078961.3:n.*59A>T
NM_024685.4:c.*59A>T MANE Select NP_078961.3:n.*59A>T
Search 100 bp 5'
Search 100 bp 3'