Canonical Allele Identifier: CA667813231
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs1169452566
MyVariant Identifiers: chr10:g.69991489G>C (hg19) chr10:g.68231732G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231732G>C , CM000672.2:g.68231732G>C GRCh38
NC_000010.10:g.69991489G>C , CM000672.1:g.69991489G>C GRCh37
NC_000010.9:g.69661495G>C NCBI36
NG_031934.1:g.5382C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.-55C>G MANE Select ENSP00000362777.3:n.-55C>G
ENST00000373673.4:c.-55C>G ENSP00000362777.3:n.-55C>G
NM_145178.3:c.-55C>G NP_660161.1:n.-55C>G
NM_145178.4:c.-55C>G MANE Select NP_660161.1:n.-55C>G
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