Canonical Allele Identifier: CA349161343
Gene: BBS5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487812G>T , CM000664.2:g.169487812G>T GRCh38
NC_000002.11:g.170344322G>T , CM000664.1:g.170344322G>T GRCh37
NC_000002.10:g.170052568G>T NCBI36
NG_011567.1:g.13317G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.215G>T MANE Select ENSP00000295240.3:p.Gly72Val
ENST00000295240.7:c.215G>T ENSP00000295240.3:p.Gly72Val
ENST00000392663.6:c.215G>T ENSP00000376431.2:p.Gly72Val
ENST00000443151.1:c.143-175G>T ENSP00000406182.1:n.143-175G>T
ENST00000475571.1:n.51G>T
ENST00000513963.1:c.215G>T ENSP00000424363.1:p.Gly72Val
NM_152384.2:c.215G>T NP_689597.1:p.Gly72Val
NM_152384.3:c.215G>T MANE Select NP_689597.1:p.Gly72Val