Canonical Allele Identifier: CA5523342
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516555
ClinVar RCV Id: RCV002026688
dbSNP Id: rs761994815
ExAC: 10:69991106 C / T
gnomAD v2: 10-69991106-C-T
gnomAD v3: 10-68231349-C-T
gnomAD v4: 10-68231349-C-T
MyVariant Identifiers: chr10:g.69991106C>T (hg19) chr10:g.68231349C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231349C>T , CM000672.2:g.68231349C>T GRCh38
NC_000010.10:g.69991106C>T , CM000672.1:g.69991106C>T GRCh37
NC_000010.9:g.69661112C>T NCBI36
NG_031934.1:g.5765G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.329G>A MANE Select ENSP00000362777.3:p.Gly110Asp
ENST00000373673.4:c.329G>A ENSP00000362777.3:p.Gly110Asp
NM_145178.3:c.329G>A NP_660161.1:p.Gly110Asp
NM_145178.4:c.329G>A MANE Select NP_660161.1:p.Gly110Asp
Search 100 bp 5'
Search 100 bp 3'