Canonical Allele Identifier: CA376837761
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1418004
ClinVar RCV Id: RCV001930807
dbSNP Id: rs2134380823
gnomAD v4: 10-68231625-G-T
MyVariant Identifiers: chr10:g.69991382G>T (hg19) chr10:g.68231625G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231625G>T , CM000672.2:g.68231625G>T GRCh38
NC_000010.10:g.69991382G>T , CM000672.1:g.69991382G>T GRCh37
NC_000010.9:g.69661388G>T NCBI36
NG_031934.1:g.5489C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.53C>A MANE Select ENSP00000362777.3:p.Pro18Gln
ENST00000373673.4:c.53C>A ENSP00000362777.3:p.Pro18Gln
NM_145178.3:c.53C>A NP_660161.1:p.Pro18Gln
NM_145178.4:c.53C>A MANE Select NP_660161.1:p.Pro18Gln
Search 100 bp 5'
Search 100 bp 3'