Canonical Allele Identifier: CA5523333
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs757008955
ExAC: 10:69991069 G / A
gnomAD v2: 10-69991069-G-A
gnomAD v4: 10-68231312-G-A
MyVariant Identifiers: chr10:g.69991069G>A (hg19) chr10:g.68231312G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231312G>A , CM000672.2:g.68231312G>A GRCh38
NC_000010.10:g.69991069G>A , CM000672.1:g.69991069G>A GRCh37
NC_000010.9:g.69661075G>A NCBI36
NG_031934.1:g.5802C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.366C>T MANE Select ENSP00000362777.3:p.Leu122=
ENST00000373673.4:c.366C>T ENSP00000362777.3:p.Leu122=
NM_145178.3:c.366C>T NP_660161.1:p.Leu122=
NM_145178.4:c.366C>T MANE Select NP_660161.1:p.Leu122=
Search 100 bp 5'
Search 100 bp 3'