Canonical Allele Identifier: CA401757553

Gene: MIB1

Linked Data

• dbSNP Id: rs1336438520
• MyVariant Identifiers: chr18:g.19395587G>A (hg19) ; chr18:g.21815626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21815626G>A , CM000680.2:g.21815626G>A	GRCh38
NC_000018.9:g.19395587G>A , CM000680.1:g.19395587G>A	GRCh37
NC_000018.8:g.17649585G>A	NCBI36
NG_033272.2:g.115670G>A , LRG_759:g.115670G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261537.7:c.1490G>A MANE Select	ENSP00000261537.6:p.Gly497Asp
ENST00000261537.6:c.1490G>A	ENSP00000261537.6:p.Gly497Asp
ENST00000577749.5:n.475G>A
ENST00000578260.1:n.293G>A
ENST00000578646.5:n.1467G>A
NM_020774.3:c.1490G>A , LRG_759t1:c.1490G>A	NP_065825.1:p.Gly497Asp
XM_011526098.1:c.20G>A	XP_011524400.1:p.Gly7Asp
XR_935234.1:n.2610G>A
XR_935235.1:n.2533G>A
XM_017025873.1:c.974G>A	XP_016881362.1:p.Gly325Asp
NM_020774.4:c.1490G>A MANE Select	NP_065825.1:p.Gly497Asp