Canonical Allele Identifier: CA358224498

Gene: BBS12

Linked Data

• ClinVar Variation Id: 1036725
• ClinVar RCV Id: RCV001339773
• dbSNP Id: rs1388311562
• MyVariant Identifiers: chr4:g.123664195A>G (hg19) ; chr4:g.122743040A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122743040A>G , CM000666.2:g.122743040A>G	GRCh38
NC_000004.11:g.123664195A>G , CM000666.1:g.123664195A>G	GRCh37
NC_000004.10:g.123883645A>G	NCBI36
NG_021203.1:g.15339A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314218.8:c.1148A>G MANE Select	ENSP00000319062.3:p.Asp383Gly
ENST00000314218.7:c.1148A>G	ENSP00000319062.3:p.Asp383Gly
ENST00000542236.5:c.1148A>G	ENSP00000438273.1:p.Asp383Gly
NM_001178007.1:c.1148A>G	NP_001171478.1:p.Asp383Gly
NM_152618.2:c.1148A>G	NP_689831.2:p.Asp383Gly
XM_011531680.1:c.1148A>G	XP_011529982.1:p.Asp383Gly
XM_011531680.2:c.1148A>G	XP_011529982.1:p.Asp383Gly
XM_017007831.1:c.1148A>G	XP_016863320.1:p.Asp383Gly
NM_152618.3:c.1148A>G MANE Select	NP_689831.2:p.Asp383Gly
NM_001178007.2:c.1148A>G	NP_001171478.1:p.Asp383Gly