Canonical Allele Identifier: CA376838165
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2004447
ClinVar RCV Id: RCV002816100
MyVariant Identifiers: chr10:g.69991429C>G (hg19) chr10:g.68231672C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231672C>G , CM000672.2:g.68231672C>G GRCh38
NC_000010.10:g.69991429C>G , CM000672.1:g.69991429C>G GRCh37
NC_000010.9:g.69661435C>G NCBI36
NG_031934.1:g.5442G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.6G>C MANE Select ENSP00000362777.3:p.Lys2Asn
ENST00000373673.4:c.6G>C ENSP00000362777.3:p.Lys2Asn
NM_145178.3:c.6G>C NP_660161.1:p.Lys2Asn
NM_145178.4:c.6G>C MANE Select NP_660161.1:p.Lys2Asn
Search 100 bp 5'
Search 100 bp 3'