Canonical Allele Identifier: CA441120878

Gene: BBS12

Linked Data

• MyVariant Identifiers: chr4:g.123664031T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122742876T>G , CM000666.2:g.122742876T>G	GRCh38
NC_000004.11:g.123664031T>G , CM000666.1:g.123664031T>G	GRCh37
NC_000004.10:g.123883481T>G	NCBI36
NG_021203.1:g.15175T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314218.8:c.984T>G MANE Select	ENSP00000319062.3:p.Ser328=
ENST00000314218.7:c.984T>G	ENSP00000319062.3:p.Ser328=
ENST00000542236.5:c.984T>G	ENSP00000438273.1:p.Ser328=
NM_001178007.1:c.984T>G	NP_001171478.1:p.Ser328=
NM_152618.2:c.984T>G	NP_689831.2:p.Ser328=
XM_011531680.1:c.984T>G	XP_011529982.1:p.Ser328=
XM_011531680.2:c.984T>G	XP_011529982.1:p.Ser328=
XM_017007831.1:c.984T>G	XP_016863320.1:p.Ser328=
NM_152618.3:c.984T>G MANE Select	NP_689831.2:p.Ser328=
NM_001178007.2:c.984T>G	NP_001171478.1:p.Ser328=