Canonical Allele Identifier: CA2289384921
Gene: MIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21815724C= , CM000680.2:g.21815724C= GRCh38
NC_000018.9:g.19395685C= , CM000680.1:g.19395685C= GRCh37
NC_000018.8:g.17649683C= NCBI36
NG_033272.2:g.115768C= , LRG_759:g.115768C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261537.7:c.1588C= MANE Select ENSP00000261537.6:p.Arg530=
ENST00000261537.6:c.1588C= ENSP00000261537.6:p.Arg530=
ENST00000577749.5:n.573C=
ENST00000578260.1:n.391C=
ENST00000578646.5:n.1565C=
NM_020774.3:c.1588C= , LRG_759t1:c.1588C= NP_065825.1:p.Arg530=
XM_011526098.1:c.118C= XP_011524400.1:p.Arg40=
XM_017025873.1:c.1072C= XP_016881362.1:p.Arg358=
NM_020774.4:c.1588C= MANE Select NP_065825.1:p.Arg530=