Canonical Allele Identifier: CA429922327

Gene: BBS5

Linked Data

• MyVariant Identifiers: chr2:g.170344350A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169487840A>T , CM000664.2:g.169487840A>T	GRCh38
NC_000002.11:g.170344350A>T , CM000664.1:g.170344350A>T	GRCh37
NC_000002.10:g.170052596A>T	NCBI36
NG_011567.1:g.13345A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295240.8:c.243A>T MANE Select	ENSP00000295240.3:p.Thr81=
ENST00000295240.7:c.243A>T	ENSP00000295240.3:p.Thr81=
ENST00000392663.6:c.243A>T	ENSP00000376431.2:p.Thr81=
ENST00000443151.1:c.143-147A>T	ENSP00000406182.1:n.143-147A>T
ENST00000475571.1:n.79A>T
ENST00000513963.1:c.243A>T	ENSP00000424363.1:p.Thr81=
NM_152384.2:c.243A>T	NP_689597.1:p.Thr81=
NM_152384.3:c.243A>T MANE Select	NP_689597.1:p.Thr81=