Canonical Allele Identifier: CA441120788
Gene: BBS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1124484
ClinVar RCV Id: RCV001455843
dbSNP Id: rs2150736872
MyVariant Identifiers: chr4:g.123664145T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122742990T>C , CM000666.2:g.122742990T>C GRCh38
NC_000004.11:g.123664145T>C , CM000666.1:g.123664145T>C GRCh37
NC_000004.10:g.123883595T>C NCBI36
NG_021203.1:g.15289T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000314218.8:c.1098T>C MANE Select ENSP00000319062.3:p.Asn366=
ENST00000314218.7:c.1098T>C ENSP00000319062.3:p.Asn366=
ENST00000542236.5:c.1098T>C ENSP00000438273.1:p.Asn366=
NM_001178007.1:c.1098T>C NP_001171478.1:p.Asn366=
NM_152618.2:c.1098T>C NP_689831.2:p.Asn366=
XM_011531680.1:c.1098T>C XP_011529982.1:p.Asn366=
XM_011531680.2:c.1098T>C XP_011529982.1:p.Asn366=
XM_017007831.1:c.1098T>C XP_016863320.1:p.Asn366=
NM_152618.3:c.1098T>C MANE Select NP_689831.2:p.Asn366=
NM_001178007.2:c.1098T>C NP_001171478.1:p.Asn366=