Canonical Allele Identifier: CA376835328
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991064A>G (hg19) chr10:g.68231307A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231307A>G , CM000672.2:g.68231307A>G GRCh38
NC_000010.10:g.69991064A>G , CM000672.1:g.69991064A>G GRCh37
NC_000010.9:g.69661070A>G NCBI36
NG_031934.1:g.5807T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.371T>C MANE Select ENSP00000362777.3:p.Phe124Ser
ENST00000373673.4:c.371T>C ENSP00000362777.3:p.Phe124Ser
NM_145178.3:c.371T>C NP_660161.1:p.Phe124Ser
NM_145178.4:c.371T>C MANE Select NP_660161.1:p.Phe124Ser
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Search 100 bp 3'