Canonical Allele Identifier: CA376836881

Gene: ATOH7

Linked Data

• dbSNP Id: rs1441622262
• gnomAD v3: 10-68231490-A-C
• gnomAD v4: 10-68231490-A-C
• MyVariant Identifiers: chr10:g.69991247A>C (hg19) ; chr10:g.68231490A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231490A>C , CM000672.2:g.68231490A>C	GRCh38
NC_000010.10:g.69991247A>C , CM000672.1:g.69991247A>C	GRCh37
NC_000010.9:g.69661253A>C	NCBI36
NG_031934.1:g.5624T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.188T>G MANE Select	ENSP00000362777.3:p.Leu63Ter
ENST00000373673.4:c.188T>G	ENSP00000362777.3:p.Leu63Ter
NM_145178.3:c.188T>G	NP_660161.1:p.Leu63Ter
NM_145178.4:c.188T>G MANE Select	NP_660161.1:p.Leu63Ter