Canonical Allele Identifier: CA469801411
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs1013711090
MyVariant Identifiers: chr10:g.69991387T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231630T>G , CM000672.2:g.68231630T>G GRCh38
NC_000010.10:g.69991387T>G , CM000672.1:g.69991387T>G GRCh37
NC_000010.9:g.69661393T>G NCBI36
NG_031934.1:g.5484A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.48A>C MANE Select ENSP00000362777.3:p.Ala16=
ENST00000373673.4:c.48A>C ENSP00000362777.3:p.Ala16=
NM_145178.3:c.48A>C NP_660161.1:p.Ala16=
NM_145178.4:c.48A>C MANE Select NP_660161.1:p.Ala16=
Search 100 bp 5'
Search 100 bp 3'