Canonical Allele Identifier: CA1917241662
Gene: ATOH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231659T= , CM000672.2:g.68231659T= GRCh38
NC_000010.10:g.69991416T= , CM000672.1:g.69991416T= GRCh37
NC_000010.9:g.69661422T= NCBI36
NG_031934.1:g.5455A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.19A= MANE Select ENSP00000362777.3:p.Ser7=
ENST00000373673.4:c.19A= ENSP00000362777.3:p.Ser7=
NM_145178.3:c.19A= NP_660161.1:p.Ser7=
NM_145178.4:c.19A= MANE Select NP_660161.1:p.Ser7=
Search 100 bp 5'
Search 100 bp 3'