Canonical Allele Identifier: CA296993604
Community Standard Title: NM_020774.4(MIB1):c.1238-309T>A
Gene: MIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21799532T>A , CM000680.2:g.21799532T>A GRCh38
NC_000018.9:g.19379493T>A , CM000680.1:g.19379493T>A GRCh37
NC_000018.8:g.17633491T>A NCBI36
NG_033272.2:g.99576T>A , LRG_759:g.99576T>A

Transcript Alleles

HGVS Amino-acid Change
NM_020774.4:c.1238-309T>A MANE Select NP_065825.1:n.1238-309T>A
ENST00000261537.7:c.1238-309T>A MANE Select ENSP00000261537.6:n.1238-309T>A
NM_020774.3:c.1238-309T>A , LRG_759t1:c.1238-309T>A NP_065825.1:n.1238-309T>A
ENST00000261537.6:c.1238-309T>A ENSP00000261537.6:n.1238-309T>A
ENST00000577749.5:n.146-309T>A
ENST00000578646.5:n.1215-309T>A
XM_017025873.1:c.722-309T>A XP_016881362.1:n.722-309T>A
XM_017025874.1:c.1238-309T>A XP_016881363.1:n.1238-309T>A
XM_017025875.1:c.1238-309T>A XP_016881364.1:n.1238-309T>A
XR_935234.1:n.2029-309T>A
XR_935235.1:n.2029-309T>A