Canonical Allele Identifier: CA8907924
Gene: MIB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 392832
ClinVar RCV Id: RCV000432654
dbSNP Id: rs777854951

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21741710G>T , CM000680.2:g.21741710G>T GRCh38
NC_000018.9:g.19321671G>T , CM000680.1:g.19321671G>T GRCh37
NC_000018.8:g.17575669G>T NCBI36
NG_033272.2:g.41754G>T , LRG_759:g.41754G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261537.7:c.127G>T MANE Select ENSP00000261537.6:p.Glu43Ter
ENST00000261537.6:c.127G>T ENSP00000261537.6:p.Glu43Ter
ENST00000578646.5:n.168-24062G>T
NM_020774.3:c.127G>T , LRG_759t1:c.127G>T NP_065825.1:p.Glu43Ter
XR_935234.1:n.918G>T
XR_935235.1:n.918G>T
XM_017025874.1:c.127G>T XP_016881363.1:p.Glu43Ter
XM_017025875.1:c.127G>T XP_016881364.1:p.Glu43Ter
NM_020774.4:c.127G>T MANE Select NP_065825.1:p.Glu43Ter