Canonical Allele Identifier: CA2661828165
Gene: BBS5 HGNC NCBI

Linked Data

dbSNP Id: rs2105297713
gnomAD v4: 2-169492830-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169492830C>A , CM000664.2:g.169492830C>A GRCh38
NC_000002.11:g.170349340C>A , CM000664.1:g.170349340C>A GRCh37
NC_000002.10:g.170057586C>A NCBI36
NG_011567.1:g.18335C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.387-44C>A MANE Select ENSP00000295240.3:n.387-44C>A
ENST00000295240.7:c.387-44C>A ENSP00000295240.3:n.387-44C>A
ENST00000392663.6:c.387-44C>A ENSP00000376431.2:n.387-44C>A
ENST00000443151.1:c.*109-44C>A ENSP00000406182.1:n.*109-44C>A
ENST00000475571.1:n.354-44C>A
ENST00000513963.1:c.387-44C>A ENSP00000424363.1:n.387-44C>A
NM_152384.2:c.387-44C>A NP_689597.1:n.387-44C>A
NM_152384.3:c.387-44C>A MANE Select NP_689597.1:n.387-44C>A
Search 100 bp 5'
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