Canonical Allele Identifier: CA469826819

Gene: ATOH7

Linked Data

• dbSNP Id: rs1348145163
• gnomAD v2: 10-69991063-G-A
• gnomAD v4: 10-68231306-G-A
• MyVariant Identifiers: chr10:g.69991063G>A (hg19) ; chr10:g.68231306G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231306G>A , CM000672.2:g.68231306G>A	GRCh38
NC_000010.10:g.69991063G>A , CM000672.1:g.69991063G>A	GRCh37
NC_000010.9:g.69661069G>A	NCBI36
NG_031934.1:g.5808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.372C>T MANE Select	ENSP00000362777.3:p.Phe124=
ENST00000373673.4:c.372C>T	ENSP00000362777.3:p.Phe124=
NM_145178.3:c.372C>T	NP_660161.1:p.Phe124=
NM_145178.4:c.372C>T MANE Select	NP_660161.1:p.Phe124=