Canonical Allele Identifier: CA469826839
Gene: ATOH7 HGNC NCBI

Linked Data

gnomAD v4: 10-68231345-G-C
COSMIC: COSM3807512
MyVariant Identifiers: chr10:g.69991102G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231345G>C , CM000672.2:g.68231345G>C GRCh38
NC_000010.10:g.69991102G>C , CM000672.1:g.69991102G>C GRCh37
NC_000010.9:g.69661108G>C NCBI36
NG_031934.1:g.5769C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.333C>G MANE Select ENSP00000362777.3:p.Leu111=
ENST00000373673.4:c.333C>G ENSP00000362777.3:p.Leu111=
NM_145178.3:c.333C>G NP_660161.1:p.Leu111=
NM_145178.4:c.333C>G MANE Select NP_660161.1:p.Leu111=
Search 100 bp 5'
Search 100 bp 3'