Canonical Allele Identifier: CA376835264
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1897005
ClinVar RCV Id: RCV002576174
gnomAD v4: 10-68231295-T-G
MyVariant Identifiers: chr10:g.69991052T>G (hg19) chr10:g.68231295T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231295T>G , CM000672.2:g.68231295T>G GRCh38
NC_000010.10:g.69991052T>G , CM000672.1:g.69991052T>G GRCh37
NC_000010.9:g.69661058T>G NCBI36
NG_031934.1:g.5819A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.383A>C MANE Select ENSP00000362777.3:p.Lys128Thr
ENST00000373673.4:c.383A>C ENSP00000362777.3:p.Lys128Thr
NM_145178.3:c.383A>C NP_660161.1:p.Lys128Thr
NM_145178.4:c.383A>C MANE Select NP_660161.1:p.Lys128Thr
Search 100 bp 5'
Search 100 bp 3'