Canonical Allele Identifier: CA376835526
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991097C>T (hg19) chr10:g.68231340C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231340C>T , CM000672.2:g.68231340C>T GRCh38
NC_000010.10:g.69991097C>T , CM000672.1:g.69991097C>T GRCh37
NC_000010.9:g.69661103C>T NCBI36
NG_031934.1:g.5774G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.338G>A MANE Select ENSP00000362777.3:p.Cys113Tyr
ENST00000373673.4:c.338G>A ENSP00000362777.3:p.Cys113Tyr
NM_145178.3:c.338G>A NP_660161.1:p.Cys113Tyr
NM_145178.4:c.338G>A MANE Select NP_660161.1:p.Cys113Tyr
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