Canonical Allele Identifier: CA376837667
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1924592
ClinVar RCV Id: RCV002613892
dbSNP Id: rs2044028234
gnomAD v4: 10-68231610-G-T
MyVariant Identifiers: chr10:g.69991367G>T (hg19) chr10:g.68231610G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231610G>T , CM000672.2:g.68231610G>T GRCh38
NC_000010.10:g.69991367G>T , CM000672.1:g.69991367G>T GRCh37
NC_000010.9:g.69661373G>T NCBI36
NG_031934.1:g.5504C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.68C>A MANE Select ENSP00000362777.3:p.Thr23Asn
ENST00000373673.4:c.68C>A ENSP00000362777.3:p.Thr23Asn
NM_145178.3:c.68C>A NP_660161.1:p.Thr23Asn
NM_145178.4:c.68C>A MANE Select NP_660161.1:p.Thr23Asn
Search 100 bp 5'
Search 100 bp 3'