Canonical Allele Identifier: CA401758232
Gene: MIB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.19395698T>C (hg19) chr18:g.21815737T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21815737T>C , CM000680.2:g.21815737T>C GRCh38
NC_000018.9:g.19395698T>C , CM000680.1:g.19395698T>C GRCh37
NC_000018.8:g.17649696T>C NCBI36
NG_033272.2:g.115781T>C , LRG_759:g.115781T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261537.7:c.1601T>C MANE Select ENSP00000261537.6:p.Leu534Pro
ENST00000261537.6:c.1601T>C ENSP00000261537.6:p.Leu534Pro
ENST00000577749.5:n.586T>C
ENST00000578260.1:n.404T>C
ENST00000578646.5:n.1578T>C
NM_020774.3:c.1601T>C , LRG_759t1:c.1601T>C NP_065825.1:p.Leu534Pro
XM_011526098.1:c.131T>C XP_011524400.1:p.Leu44Pro
XM_017025873.1:c.1085T>C XP_016881362.1:p.Leu362Pro
NM_020774.4:c.1601T>C MANE Select NP_065825.1:p.Leu534Pro
Search 100 bp 5'
Search 100 bp 3'