Canonical Allele Identifier: CA8908409
Gene: MIB1 HGNC NCBI
MIR133A1HG HGNC NCBI
MyVariant.info:
GRCh38 chr18:g.21828989C>T
GRCh37 chr18:g.19408950C>T
gnomAD v2:
18:19408950 C / T
gnomAD v3:
18:21828989 C / T
gnomAD v4:
chr18-21828989-C-T
Joint Max Group AF 0.97722431 (NFE)
Genomes Max Group AF 0.97450556 (NFE)
Exomes Max Group AF 0.97650756 (NFE)
dbSNP:
9989532
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21828989C>T , CM000680.2:g.21828989C>T GRCh38
NC_000018.9:g.19408950C>T , CM000680.1:g.19408950C>T GRCh37
NC_000018.8:g.17662948C>T NCBI36
NG_033272.2:g.129033C>T , LRG_759:g.129033C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695486.1:n.582+9343C>T (MIB1)
ENST00000261537.7:c.1829+9343C>T (MIB1) MANE Select ENSP00000261537.6:n.1829+9343C>T
ENST00000261537.6:c.1829+9343C>T (MIB1) ENSP00000261537.6:n.1829+9343C>T
ENST00000578646.5:n.1806+9343C>T (MIB1)
NM_020774.3:c.1829+9343C>T , LRG_759t1:c.1829+9343C>T (MIB1) NP_065825.1:n.1829+9343C>T
NR_110369.1:n.724G>A (MIR133A1HG)
XM_011526098.1:c.359+9343C>T (MIB1) XP_011524400.1:n.359+9343C>T
XM_017025873.1:c.1313+9343C>T (MIB1) XP_016881362.1:n.1313+9343C>T
NM_020774.4:c.1829+9343C>T (MIB1) MANE Select NP_065825.1:n.1829+9343C>T
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