Canonical Allele Identifier: CA5523341
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167445
ClinVar RCV Id: RCV001516659
dbSNP Id: rs201955526
ExAC: 10:69991099 G / A
gnomAD v2: 10-69991099-G-A
gnomAD v3: 10-68231342-G-A
gnomAD v4: 10-68231342-G-A
MyVariant Identifiers: chr10:g.69991099G>A (hg19) chr10:g.68231342G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231342G>A , CM000672.2:g.68231342G>A GRCh38
NC_000010.10:g.69991099G>A , CM000672.1:g.69991099G>A GRCh37
NC_000010.9:g.69661105G>A NCBI36
NG_031934.1:g.5772C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.336C>T MANE Select ENSP00000362777.3:p.His112=
ENST00000373673.4:c.336C>T ENSP00000362777.3:p.His112=
NM_145178.3:c.336C>T NP_660161.1:p.His112=
NM_145178.4:c.336C>T MANE Select NP_660161.1:p.His112=
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Search 100 bp 3'