Canonical Allele Identifier: CA376837596
Gene: ATOH7 HGNC NCBI

Linked Data

gnomAD v4: 10-68231601-G-T
MyVariant Identifiers: chr10:g.69991358G>T (hg19) chr10:g.68231601G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231601G>T , CM000672.2:g.68231601G>T GRCh38
NC_000010.10:g.69991358G>T , CM000672.1:g.69991358G>T GRCh37
NC_000010.9:g.69661364G>T NCBI36
NG_031934.1:g.5513C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.77C>A MANE Select ENSP00000362777.3:p.Ala26Glu
ENST00000373673.4:c.77C>A ENSP00000362777.3:p.Ala26Glu
NM_145178.3:c.77C>A NP_660161.1:p.Ala26Glu
NM_145178.4:c.77C>A MANE Select NP_660161.1:p.Ala26Glu
Search 100 bp 5'
Search 100 bp 3'