Canonical Allele Identifier: CA376837758

Gene: ATOH7

Linked Data

• ClinVar Variation Id: 2088238
• ClinVar RCV Id: RCV003009963
• gnomAD v4: 10-68231625-G-C
• MyVariant Identifiers: chr10:g.69991382G>C (hg19) ; chr10:g.68231625G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231625G>C , CM000672.2:g.68231625G>C	GRCh38
NC_000010.10:g.69991382G>C , CM000672.1:g.69991382G>C	GRCh37
NC_000010.9:g.69661388G>C	NCBI36
NG_031934.1:g.5489C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.53C>G MANE Select	ENSP00000362777.3:p.Pro18Arg
ENST00000373673.4:c.53C>G	ENSP00000362777.3:p.Pro18Arg
NM_145178.3:c.53C>G	NP_660161.1:p.Pro18Arg
NM_145178.4:c.53C>G MANE Select	NP_660161.1:p.Pro18Arg