Canonical Allele Identifier: CA376837841

Gene: ATOH7

Linked Data

• ClinVar Variation Id: 953540
• ClinVar RCV Id: RCV001225846
• dbSNP Id: rs2044028480
• gnomAD v3: 10-68231635-C-A
• gnomAD v4: 10-68231635-C-A
• MyVariant Identifiers: chr10:g.69991392C>A (hg19) ; chr10:g.68231635C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231635C>A , CM000672.2:g.68231635C>A	GRCh38
NC_000010.10:g.69991392C>A , CM000672.1:g.69991392C>A	GRCh37
NC_000010.9:g.69661398C>A	NCBI36
NG_031934.1:g.5479G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.43G>T MANE Select	ENSP00000362777.3:p.Val15Phe
ENST00000373673.4:c.43G>T	ENSP00000362777.3:p.Val15Phe
NM_145178.3:c.43G>T	NP_660161.1:p.Val15Phe
NM_145178.4:c.43G>T MANE Select	NP_660161.1:p.Val15Phe