Canonical Allele Identifier: CA469801417
Gene: ATOH7 HGNC NCBI

Linked Data

gnomAD v4: 10-68231633-A-G
MyVariant Identifiers: chr10:g.69991390A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231633A>G , CM000672.2:g.68231633A>G GRCh38
NC_000010.10:g.69991390A>G , CM000672.1:g.69991390A>G GRCh37
NC_000010.9:g.69661396A>G NCBI36
NG_031934.1:g.5481T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.45T>C MANE Select ENSP00000362777.3:p.Val15=
ENST00000373673.4:c.45T>C ENSP00000362777.3:p.Val15=
NM_145178.3:c.45T>C NP_660161.1:p.Val15=
NM_145178.4:c.45T>C MANE Select NP_660161.1:p.Val15=
Search 100 bp 5'
Search 100 bp 3'