Canonical Allele Identifier: CA8908262

Gene: MIB1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21799898A>G , CM000680.2:g.21799898A>G	GRCh38
NC_000018.9:g.19379859A>G , CM000680.1:g.19379859A>G	GRCh37
NC_000018.8:g.17633857A>G	NCBI36
NG_033272.2:g.99942A>G , LRG_759:g.99942A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020774.4:c.1295A>G MANE Select	NP_065825.1:p.Asn432Ser
ENST00000261537.7:c.1295A>G MANE Select	ENSP00000261537.6:p.Asn432Ser
NM_020774.3:c.1295A>G , LRG_759t1:c.1295A>G	NP_065825.1:p.Asn432Ser
ENST00000261537.6:c.1295A>G	ENSP00000261537.6:p.Asn432Ser
ENST00000577749.5:n.203A>G
ENST00000578646.5:n.1272A>G
XM_017025873.1:c.779A>G	XP_016881362.1:p.Asn260Ser
XM_017025874.1:c.1295A>G	XP_016881363.1:p.Asn432Ser
XM_017025875.1:c.1295A>G	XP_016881364.1:p.Asn432Ser
XR_935234.1:n.2086A>G
XR_935235.1:n.2086A>G