Canonical Allele Identifier: CA1917241502
Gene: ATOH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231372G= , CM000672.2:g.68231372G= GRCh38
NC_000010.10:g.69991129G= , CM000672.1:g.69991129G= GRCh37
NC_000010.9:g.69661135G= NCBI36
NG_031934.1:g.5742C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.306C= MANE Select ENSP00000362777.3:p.Phe102=
ENST00000373673.4:c.306C= ENSP00000362777.3:p.Phe102=
NM_145178.3:c.306C= NP_660161.1:p.Phe102=
NM_145178.4:c.306C= MANE Select NP_660161.1:p.Phe102=
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