Canonical Allele Identifier: CA376835639
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs1190972084
gnomAD v3: 10-68231359-C-A
gnomAD v4: 10-68231359-C-A
MyVariant Identifiers: chr10:g.69991116C>A (hg19) chr10:g.68231359C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231359C>A , CM000672.2:g.68231359C>A GRCh38
NC_000010.10:g.69991116C>A , CM000672.1:g.69991116C>A GRCh37
NC_000010.9:g.69661122C>A NCBI36
NG_031934.1:g.5755G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.319G>T MANE Select ENSP00000362777.3:p.Asp107Tyr
ENST00000373673.4:c.319G>T ENSP00000362777.3:p.Asp107Tyr
NM_145178.3:c.319G>T NP_660161.1:p.Asp107Tyr
NM_145178.4:c.319G>T MANE Select NP_660161.1:p.Asp107Tyr
Search 100 bp 5'
Search 100 bp 3'