Canonical Allele Identifier: CA8908277
Community Standard Title: NM_020774.4(MIB1):c.1372-11A>T
Gene: MIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21803896A>T , CM000680.2:g.21803896A>T GRCh38
NC_000018.9:g.19383857A>T , CM000680.1:g.19383857A>T GRCh37
NC_000018.8:g.17637855A>T NCBI36
NG_033272.2:g.103940A>T , LRG_759:g.103940A>T

Transcript Alleles

HGVS Amino-acid Change
NM_020774.4:c.1372-11A>T MANE Select NP_065825.1:n.1372-11A>T
ENST00000261537.7:c.1372-11A>T MANE Select ENSP00000261537.6:n.1372-11A>T
NM_020774.3:c.1372-11A>T , LRG_759t1:c.1372-11A>T NP_065825.1:n.1372-11A>T
ENST00000261537.6:c.1372-11A>T ENSP00000261537.6:n.1372-11A>T
ENST00000577749.5:n.280-11A>T
ENST00000578260.1:n.164A>T
ENST00000578646.5:n.1349-11A>T
XM_017025873.1:c.856-11A>T XP_016881362.1:n.856-11A>T
XM_017025874.1:c.1372-11A>T XP_016881363.1:n.1372-11A>T
XM_017025875.1:c.1372-11A>T XP_016881364.1:n.1372-11A>T
XR_935234.1:n.2163-11A>T
XR_935235.1:n.2163-11A>T