Canonical Allele Identifier: CA376835258

Gene: ATOH7

Linked Data

• dbSNP Id: rs2044024992
• gnomAD v3: 10-68231295-T-C
• gnomAD v4: 10-68231295-T-C
• MyVariant Identifiers: chr10:g.69991052T>C (hg19) ; chr10:g.68231295T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231295T>C , CM000672.2:g.68231295T>C	GRCh38
NC_000010.10:g.69991052T>C , CM000672.1:g.69991052T>C	GRCh37
NC_000010.9:g.69661058T>C	NCBI36
NG_031934.1:g.5819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.383A>G MANE Select	ENSP00000362777.3:p.Lys128Arg
ENST00000373673.4:c.383A>G	ENSP00000362777.3:p.Lys128Arg
NM_145178.3:c.383A>G	NP_660161.1:p.Lys128Arg
NM_145178.4:c.383A>G MANE Select	NP_660161.1:p.Lys128Arg