Canonical Allele Identifier: CA469801415
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991390A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231633A>C , CM000672.2:g.68231633A>C GRCh38
NC_000010.10:g.69991390A>C , CM000672.1:g.69991390A>C GRCh37
NC_000010.9:g.69661396A>C NCBI36
NG_031934.1:g.5481T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.45T>G MANE Select ENSP00000362777.3:p.Val15=
ENST00000373673.4:c.45T>G ENSP00000362777.3:p.Val15=
NM_145178.3:c.45T>G NP_660161.1:p.Val15=
NM_145178.4:c.45T>G MANE Select NP_660161.1:p.Val15=
Search 100 bp 5'
Search 100 bp 3'