Canonical Allele Identifier: CA401758200

Gene: MIB1

Linked Data

• MyVariant Identifiers: chr18:g.19395690G>T (hg19) ; chr18:g.21815729G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21815729G>T , CM000680.2:g.21815729G>T	GRCh38
NC_000018.9:g.19395690G>T , CM000680.1:g.19395690G>T	GRCh37
NC_000018.8:g.17649688G>T	NCBI36
NG_033272.2:g.115773G>T , LRG_759:g.115773G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261537.7:c.1593G>T MANE Select	ENSP00000261537.6:p.Gln531His
ENST00000261537.6:c.1593G>T	ENSP00000261537.6:p.Gln531His
ENST00000577749.5:n.578G>T
ENST00000578260.1:n.396G>T
ENST00000578646.5:n.1570G>T
NM_020774.3:c.1593G>T , LRG_759t1:c.1593G>T	NP_065825.1:p.Gln531His
XM_011526098.1:c.123G>T	XP_011524400.1:p.Gln41His
XM_017025873.1:c.1077G>T	XP_016881362.1:p.Gln359His
NM_020774.4:c.1593G>T MANE Select	NP_065825.1:p.Gln531His