Canonical Allele Identifier: CA401754926

Gene: MIB1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21803952C>T , CM000680.2:g.21803952C>T	GRCh38
NC_000018.9:g.19383913C>T , CM000680.1:g.19383913C>T	GRCh37
NC_000018.8:g.17637911C>T	NCBI36
NG_033272.2:g.103996C>T , LRG_759:g.103996C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020774.4:c.1417C>T MANE Select	NP_065825.1:p.Gln473Ter
ENST00000261537.7:c.1417C>T MANE Select	ENSP00000261537.6:p.Gln473Ter
NM_020774.3:c.1417C>T , LRG_759t1:c.1417C>T	NP_065825.1:p.Gln473Ter
ENST00000261537.6:c.1417C>T	ENSP00000261537.6:p.Gln473Ter
ENST00000577749.5:n.325C>T
ENST00000578260.1:n.220C>T
ENST00000578646.5:n.1394C>T
XM_017025873.1:c.901C>T	XP_016881362.1:p.Gln301Ter
XM_017025874.1:c.1417C>T	XP_016881363.1:p.Gln473Ter
XM_017025875.1:c.1417C>T	XP_016881364.1:p.Gln473Ter
XR_935234.1:n.2208C>T
XR_935235.1:n.2208C>T