Canonical Allele Identifier: CA376837178
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs587777664
gnomAD v4: 10-68231532-T-C
MyVariant Identifiers: chr10:g.69991289T>C (hg19) chr10:g.68231532T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231532T>C , CM000672.2:g.68231532T>C GRCh38
NC_000010.10:g.69991289T>C , CM000672.1:g.69991289T>C GRCh37
NC_000010.9:g.69661295T>C NCBI36
NG_031934.1:g.5582A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.146A>G MANE Select ENSP00000362777.3:p.Glu49Gly
ENST00000373673.4:c.146A>G ENSP00000362777.3:p.Glu49Gly
NM_145178.3:c.146A>G NP_660161.1:p.Glu49Gly
NM_145178.4:c.146A>G MANE Select NP_660161.1:p.Glu49Gly
Search 100 bp 5'
Search 100 bp 3'