Canonical Allele Identifier: CA349164666
Gene: BBS5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.170349415T>A (hg19) chr2:g.169492905T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169492905T>A , CM000664.2:g.169492905T>A GRCh38
NC_000002.11:g.170349415T>A , CM000664.1:g.170349415T>A GRCh37
NC_000002.10:g.170057661T>A NCBI36
NG_011567.1:g.18410T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.418T>A MANE Select ENSP00000295240.3:p.Phe140Ile
ENST00000295240.7:c.418T>A ENSP00000295240.3:p.Phe140Ile
ENST00000392663.6:c.418T>A ENSP00000376431.2:p.Phe140Ile
ENST00000443151.1:c.*140T>A ENSP00000406182.1:n.*140T>A
ENST00000475571.1:n.385T>A
ENST00000513963.1:c.418T>A ENSP00000424363.1:p.Phe140Ile
NM_152384.2:c.418T>A NP_689597.1:p.Phe140Ile
NM_152384.3:c.418T>A MANE Select NP_689597.1:p.Phe140Ile
Search 100 bp 5'
Search 100 bp 3'