Canonical Allele Identifier: CA469801052
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991308G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231551G>A , CM000672.2:g.68231551G>A GRCh38
NC_000010.10:g.69991308G>A , CM000672.1:g.69991308G>A GRCh37
NC_000010.9:g.69661314G>A NCBI36
NG_031934.1:g.5563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.127C>T MANE Select ENSP00000362777.3:p.Leu43=
ENST00000373673.4:c.127C>T ENSP00000362777.3:p.Leu43=
NM_145178.3:c.127C>T NP_660161.1:p.Leu43=
NM_145178.4:c.127C>T MANE Select NP_660161.1:p.Leu43=
Search 100 bp 5'
Search 100 bp 3'