Canonical Allele Identifier: CA208210040

Gene: ATOH7

Linked Data

• dbSNP Id: rs562618635
• gnomAD v3: 10-68231629-G-A
• gnomAD v4: 10-68231629-G-A
• MyVariant Identifiers: chr10:g.69991386G>A (hg19) ; chr10:g.68231629G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68231629G>A , CM000672.2:g.68231629G>A	GRCh38
NC_000010.10:g.69991386G>A , CM000672.1:g.69991386G>A	GRCh37
NC_000010.9:g.69661392G>A	NCBI36
NG_031934.1:g.5485C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373673.5:c.49C>T MANE Select	ENSP00000362777.3:p.Pro17Ser
ENST00000373673.4:c.49C>T	ENSP00000362777.3:p.Pro17Ser
NM_145178.3:c.49C>T	NP_660161.1:p.Pro17Ser
NM_145178.4:c.49C>T MANE Select	NP_660161.1:p.Pro17Ser