Canonical Allele Identifier: CA469826851
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs2044025442
gnomAD v4: 10-68231351-C-A
MyVariant Identifiers: chr10:g.69991108C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231351C>A , CM000672.2:g.68231351C>A GRCh38
NC_000010.10:g.69991108C>A , CM000672.1:g.69991108C>A GRCh37
NC_000010.9:g.69661114C>A NCBI36
NG_031934.1:g.5763G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.327G>T MANE Select ENSP00000362777.3:p.Val109=
ENST00000373673.4:c.327G>T ENSP00000362777.3:p.Val109=
NM_145178.3:c.327G>T NP_660161.1:p.Val109=
NM_145178.4:c.327G>T MANE Select NP_660161.1:p.Val109=
Search 100 bp 5'
Search 100 bp 3'