Canonical Allele Identifier: CA658799006
Gene: MIB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 511952
dbSNP Id: rs1555689079

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21765766T>C , CM000680.2:g.21765766T>C GRCh38
NC_000018.9:g.19345727T>C , CM000680.1:g.19345727T>C GRCh37
NC_000018.8:g.17599725T>C NCBI36
NG_033272.2:g.65810T>C , LRG_759:g.65810T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261537.7:c.230-6T>C MANE Select ENSP00000261537.6:n.230-6T>C
ENST00000261537.6:c.230-6T>C ENSP00000261537.6:n.230-6T>C
ENST00000578646.5:n.168-6T>C
NM_020774.3:c.230-6T>C , LRG_759t1:c.230-6T>C NP_065825.1:n.230-6T>C
XR_935234.1:n.1021-6T>C
XR_935235.1:n.1021-6T>C
XM_017025874.1:c.230-6T>C XP_016881363.1:n.230-6T>C
XM_017025875.1:c.230-6T>C XP_016881364.1:n.230-6T>C
NM_020774.4:c.230-6T>C MANE Select NP_065825.1:n.230-6T>C