Canonical Allele Identifier: CA281485809

Gene: BBS2

Linked Data

• ClinVar Variation Id: 1422452
• ClinVar RCV Id: RCV001926145
• dbSNP Id: rs895169510
• MyVariant Identifiers: chr16:g.56548483C>G (hg19) ; chr16:g.56514571C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56514571C>G , CM000678.2:g.56514571C>G	GRCh38
NC_000016.9:g.56548483C>G , CM000678.1:g.56548483C>G	GRCh37
NC_000016.8:g.55105984C>G	NCBI36
NG_009312.1:g.10713G>C
NG_009312.2:g.10454G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562012.2:c.*201G>C	ENSP00000455651.2:n.*201G>C
ENST00000562059.2:n.224G>C
ENST00000565378.2:n.110G>C
ENST00000565781.6:n.241G>C
ENST00000566410.2:n.440G>C
ENST00000568104.6:c.227G>C	ENSP00000456289.1:p.Ser76Thr
ENST00000569342.6:n.400G>C
ENST00000569941.6:c.-247G>C	ENSP00000456741.2:n.-247G>C
ENST00000682001.1:n.221G>C
ENST00000682005.1:n.218G>C
ENST00000682021.1:n.237G>C
ENST00000682038.1:c.227G>C	ENSP00000508404.1:p.Ser76Thr
ENST00000682047.1:c.227G>C	ENSP00000507699.1:p.Ser76Thr
ENST00000682088.1:c.227G>C	ENSP00000508064.1:p.Ser76Thr
ENST00000682096.1:n.433G>C
ENST00000682113.1:n.200G>C
ENST00000682146.1:n.440G>C
ENST00000682187.1:c.227G>C	ENSP00000507203.1:p.Ser76Thr
ENST00000682188.1:c.227G>C	ENSP00000507655.1:p.Ser76Thr
ENST00000682201.1:n.218G>C
ENST00000682205.1:c.227G>C	ENSP00000508377.1:p.Ser76Thr
ENST00000682348.1:c.227G>C	ENSP00000506965.1:p.Ser76Thr
ENST00000682360.1:c.-371G>C	ENSP00000508007.1:n.-371G>C
ENST00000682370.1:n.433G>C
ENST00000682420.1:n.433G>C
ENST00000682429.1:c.227G>C	ENSP00000506827.1:p.Ser76Thr
ENST00000682449.1:c.227G>C	ENSP00000507836.1:p.Ser76Thr
ENST00000682470.1:c.227G>C	ENSP00000507654.1:p.Ser76Thr
ENST00000682473.1:n.192G>C
ENST00000682482.1:c.227G>C	ENSP00000507903.1:p.Ser76Thr
ENST00000682492.1:n.271G>C
ENST00000682493.1:c.227G>C	ENSP00000506778.1:p.Ser76Thr
ENST00000682543.1:c.227G>C	ENSP00000507592.1:p.Ser76Thr
ENST00000682561.1:n.236G>C
ENST00000682597.1:n.433G>C
ENST00000682658.1:c.227G>C	ENSP00000507773.1:p.Ser76Thr
ENST00000682705.1:n.433G>C
ENST00000682723.1:c.-371G>C	ENSP00000507115.1:n.-371G>C
ENST00000682735.1:c.227G>C	ENSP00000507007.1:p.Ser76Thr
ENST00000682737.1:c.-371G>C	ENSP00000506876.1:n.-371G>C
ENST00000682757.1:n.433G>C
ENST00000682855.1:c.227G>C	ENSP00000507027.1:p.Ser76Thr
ENST00000682857.1:n.440G>C
ENST00000682875.1:c.227G>C	ENSP00000507771.1:p.Ser76Thr
ENST00000682919.1:n.189G>C
ENST00000682930.1:c.152G>C	ENSP00000507981.1:p.Ser51Thr
ENST00000682948.1:n.440G>C
ENST00000682960.1:n.440G>C
ENST00000683008.1:n.433G>C
ENST00000683020.1:c.227G>C	ENSP00000507944.1:p.Ser76Thr
ENST00000683099.1:n.433G>C
ENST00000683170.1:n.371G>C
ENST00000683212.1:c.227G>C	ENSP00000507839.1:p.Ser76Thr
ENST00000683248.1:n.433G>C
ENST00000683343.1:n.218G>C
ENST00000683347.1:n.218G>C
ENST00000683384.1:c.110G>C	ENSP00000508330.1:p.Ser37Thr
ENST00000683396.1:n.433G>C
ENST00000683410.1:n.433G>C
ENST00000683485.1:n.440G>C
ENST00000683504.1:n.433G>C
ENST00000683533.1:c.-371G>C	ENSP00000508296.1:n.-371G>C
ENST00000683609.1:n.440G>C
ENST00000683644.1:c.227G>C	ENSP00000507914.1:p.Ser76Thr
ENST00000683660.1:n.440G>C
ENST00000683669.1:n.110G>C
ENST00000683690.1:c.227G>C	ENSP00000508152.1:p.Ser76Thr
ENST00000683719.1:n.210G>C
ENST00000683757.1:n.216G>C
ENST00000683858.1:c.227G>C	ENSP00000507657.1:p.Ser76Thr
ENST00000683875.1:c.118-3287G>C	ENSP00000507602.1:n.118-3287G>C
ENST00000683904.1:n.440G>C
ENST00000683910.1:n.440G>C
ENST00000683959.1:c.-371G>C	ENSP00000508309.1:n.-371G>C
ENST00000683976.1:c.227G>C	ENSP00000507183.1:p.Ser76Thr
ENST00000683978.1:n.370G>C
ENST00000683992.1:c.227G>C	ENSP00000508144.1:p.Ser76Thr
ENST00000684020.1:n.433G>C
ENST00000684044.1:n.440G>C
ENST00000684057.1:n.429G>C
ENST00000684076.1:n.398G>C
ENST00000684128.1:n.433G>C
ENST00000684194.1:n.433G>C
ENST00000684205.1:n.271G>C
ENST00000684246.1:c.227G>C	ENSP00000508273.1:p.Ser76Thr
ENST00000684402.1:n.433G>C
ENST00000684446.1:n.440G>C
ENST00000684531.1:n.460G>C
ENST00000684635.1:c.227G>C	ENSP00000507335.1:p.Ser76Thr
ENST00000684640.1:c.110G>C	ENSP00000507292.1:p.Ser37Thr
ENST00000684673.1:c.227G>C	ENSP00000507746.1:p.Ser76Thr
ENST00000684684.1:c.227G>C	ENSP00000507026.1:p.Ser76Thr
ENST00000245157.11:c.227G>C MANE Select	ENSP00000245157.5:p.Ser76Thr
ENST00000245157.9:c.227G>C	ENSP00000245157.5:p.Ser76Thr
ENST00000565378.1:n.210G>C
ENST00000565781.5:n.241G>C
ENST00000566689.5:n.218G>C
ENST00000568104.5:c.227G>C	ENSP00000456289.1:p.Ser76Thr
ENST00000569342.5:n.361G>C
ENST00000569941.5:c.-371G>C	ENSP00000456741.1:n.-371G>C
NM_031885.3:c.227G>C	NP_114091.3:p.Ser76Thr
XM_005256080.1:c.227G>C	XP_005256137.1:p.Ser76Thr
XM_005256081.1:c.227G>C	XP_005256138.1:p.Ser76Thr
XM_005256082.1:c.227G>C	XP_005256139.1:p.Ser76Thr
XM_011523251.1:c.227G>C	XP_011521553.1:p.Ser76Thr
XR_933378.1:n.460G>C
XR_933379.1:n.460G>C
XR_933380.1:n.460G>C
XM_005256080.2:c.227G>C	XP_005256137.1:p.Ser76Thr
XR_001751958.1:n.460G>C
XR_001751959.2:n.460G>C
XR_001751960.1:n.460G>C
XR_001751961.1:n.460G>C
XR_933380.2:n.460G>C
NM_031885.4:c.227G>C	NP_114091.3:p.Ser76Thr
NM_001377456.1:c.227G>C	NP_001364385.1:p.Ser76Thr
NM_031885.5:c.227G>C MANE Select	NP_114091.4:p.Ser76Thr
NR_165293.1:n.389G>C
NR_165294.1:n.389G>C
NR_165295.1:n.389G>C
NR_165296.1:n.389G>C
NR_165297.1:n.389G>C