Canonical Allele Identifier: CA376835782
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991158T>A (hg19) chr10:g.68231401T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231401T>A , CM000672.2:g.68231401T>A GRCh38
NC_000010.10:g.69991158T>A , CM000672.1:g.69991158T>A GRCh37
NC_000010.9:g.69661164T>A NCBI36
NG_031934.1:g.5713A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.277A>T MANE Select ENSP00000362777.3:p.Thr93Ser
ENST00000373673.4:c.277A>T ENSP00000362777.3:p.Thr93Ser
NM_145178.3:c.277A>T NP_660161.1:p.Thr93Ser
NM_145178.4:c.277A>T MANE Select NP_660161.1:p.Thr93Ser
Search 100 bp 5'
Search 100 bp 3'