Canonical Allele Identifier: CA1917241485
Gene: ATOH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231331A= , CM000672.2:g.68231331A= GRCh38
NC_000010.10:g.69991088A= , CM000672.1:g.69991088A= GRCh37
NC_000010.9:g.69661094A= NCBI36
NG_031934.1:g.5783T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.347T= MANE Select ENSP00000362777.3:p.Phe116=
ENST00000373673.4:c.347T= ENSP00000362777.3:p.Phe116=
NM_145178.3:c.347T= NP_660161.1:p.Phe116=
NM_145178.4:c.347T= MANE Select NP_660161.1:p.Phe116=
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