Canonical Allele Identifier: CA376837758
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2088238
ClinVar RCV Id: RCV003009963
gnomAD v4: 10-68231625-G-C
MyVariant Identifiers: chr10:g.69991382G>C (hg19) chr10:g.68231625G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231625G>C , CM000672.2:g.68231625G>C GRCh38
NC_000010.10:g.69991382G>C , CM000672.1:g.69991382G>C GRCh37
NC_000010.9:g.69661388G>C NCBI36
NG_031934.1:g.5489C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.53C>G MANE Select ENSP00000362777.3:p.Pro18Arg
ENST00000373673.4:c.53C>G ENSP00000362777.3:p.Pro18Arg
NM_145178.3:c.53C>G NP_660161.1:p.Pro18Arg
NM_145178.4:c.53C>G MANE Select NP_660161.1:p.Pro18Arg
Search 100 bp 5'
Search 100 bp 3'