Canonical Allele Identifier: CA376835888
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475147
ClinVar RCV Id: RCV001973904
dbSNP Id: rs1198341225

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231428T>C , CM000672.2:g.68231428T>C GRCh38
NC_000010.10:g.69991185T>C , CM000672.1:g.69991185T>C GRCh37
NC_000010.9:g.69661191T>C NCBI36
NG_031934.1:g.5686A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.250A>G MANE Select ENSP00000362777.3:p.Met84Val
ENST00000373673.4:c.250A>G ENSP00000362777.3:p.Met84Val
NM_145178.3:c.250A>G NP_660161.1:p.Met84Val
NM_145178.4:c.250A>G MANE Select NP_660161.1:p.Met84Val