Canonical Allele Identifier: CA469801362
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs2044028316
MyVariant Identifiers: chr10:g.69991375C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231618C>G , CM000672.2:g.68231618C>G GRCh38
NC_000010.10:g.69991375C>G , CM000672.1:g.69991375C>G GRCh37
NC_000010.9:g.69661381C>G NCBI36
NG_031934.1:g.5496G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.60G>C MANE Select ENSP00000362777.3:p.Ala20=
ENST00000373673.4:c.60G>C ENSP00000362777.3:p.Ala20=
NM_145178.3:c.60G>C NP_660161.1:p.Ala20=
NM_145178.4:c.60G>C MANE Select NP_660161.1:p.Ala20=