Canonical Allele Identifier: CA8908236
Gene: MIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21798226G>A , CM000680.2:g.21798226G>A GRCh38
NC_000018.9:g.19378187G>A , CM000680.1:g.19378187G>A GRCh37
NC_000018.8:g.17632185G>A NCBI36
NG_033272.2:g.98270G>A , LRG_759:g.98270G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261537.7:c.1235G>A MANE Select ENSP00000261537.6:p.Gly412Asp
ENST00000261537.6:c.1235G>A ENSP00000261537.6:p.Gly412Asp
ENST00000577749.5:n.143G>A
ENST00000578646.5:n.1212G>A
NM_020774.3:c.1235G>A , LRG_759t1:c.1235G>A NP_065825.1:p.Gly412Asp
XR_935234.1:n.2026G>A
XR_935235.1:n.2026G>A
XM_017025873.1:c.719G>A XP_016881362.1:p.Gly240Asp
XM_017025874.1:c.1235G>A XP_016881363.1:p.Gly412Asp
XM_017025875.1:c.1235G>A XP_016881364.1:p.Gly412Asp
NM_020774.4:c.1235G>A MANE Select NP_065825.1:p.Gly412Asp