Canonical Allele Identifier: CA1917241490
Gene: ATOH7 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.336C= MANE Select ENSP00000362777.3:p.His112=
ENST00000373673.4:c.336C= ENSP00000362777.3:p.His112=
NM_145178.3:c.336C= NP_660161.1:p.His112=
NM_145178.4:c.336C= MANE Select NP_660161.1:p.His112=
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