Canonical Allele Identifier: CA593850984
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs1305751523
gnomAD v2: 10-69991493-G-T
gnomAD v3: 10-68231736-G-T
gnomAD v4: 10-68231736-G-T
MyVariant Identifiers: chr10:g.69991493G>T (hg19) chr10:g.68231736G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231736G>T , CM000672.2:g.68231736G>T GRCh38
NC_000010.10:g.69991493G>T , CM000672.1:g.69991493G>T GRCh37
NC_000010.9:g.69661499G>T NCBI36
NG_031934.1:g.5378C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.-59C>A MANE Select ENSP00000362777.3:n.-59C>A
ENST00000373673.4:c.-59C>A ENSP00000362777.3:n.-59C>A
NM_145178.3:c.-59C>A NP_660161.1:n.-59C>A
NM_145178.4:c.-59C>A MANE Select NP_660161.1:n.-59C>A
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