Canonical Allele Identifier: CA3069228

Gene: BBS12

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122741952A>G , CM000666.2:g.122741952A>G	GRCh38
NC_000004.11:g.123663107A>G , CM000666.1:g.123663107A>G	GRCh37
NC_000004.10:g.123882557A>G	NCBI36
NG_021203.1:g.14251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314218.8:c.60A>G MANE Select	ENSP00000319062.3:p.Ser20=
ENST00000314218.7:c.60A>G	ENSP00000319062.3:p.Ser20=
ENST00000433287.1:c.60A>G	ENSP00000398912.1:p.Ser20=
ENST00000542236.5:c.60A>G	ENSP00000438273.1:p.Ser20=
NM_001178007.1:c.60A>G	NP_001171478.1:p.Ser20=
NM_152618.2:c.60A>G	NP_689831.2:p.Ser20=
XM_011531680.1:c.60A>G	XP_011529982.1:p.Ser20=
XM_011531680.2:c.60A>G	XP_011529982.1:p.Ser20=
XM_017007831.1:c.60A>G	XP_016863320.1:p.Ser20=
NM_152618.3:c.60A>G MANE Select	NP_689831.2:p.Ser20=
NM_001178007.2:c.60A>G	NP_001171478.1:p.Ser20=