Canonical Allele Identifier: CA13222958
Gene: ATOH7 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.68232096A>G
GRCh37 chr10:g.69991853A>G
gnomAD v2:
10:69991853 A / G
gnomAD v3:
10:68232096 A / G
gnomAD v4:
chr10-68232096-A-G
Joint Max Group AF 0.7449666 (NFE)
Genomes Max Group AF 0.74490419 (NFE)
Exomes Max Group AF 0.6833979 (NFE)
ClinVar RCV:
RCV001635868
ClinVar Variation:
1237376
dbSNP:
7916697
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68232096A>G , CM000672.2:g.68232096A>G GRCh38
NC_000010.10:g.69991853A>G , CM000672.1:g.69991853A>G GRCh37
NC_000010.9:g.69661859A>G NCBI36
NG_031934.1:g.5018T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.-419T>C MANE Select ENSP00000362777.3:n.-419T>C
ENST00000373673.4:c.-419T>C ENSP00000362777.3:n.-419T>C
NM_145178.3:c.-419T>C NP_660161.1:n.-419T>C
NM_145178.4:c.-419T>C MANE Select NP_660161.1:n.-419T>C
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