Canonical Allele Identifier: CA376835907
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991194T>C (hg19) chr10:g.68231437T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231437T>C , CM000672.2:g.68231437T>C GRCh38
NC_000010.10:g.69991194T>C , CM000672.1:g.69991194T>C GRCh37
NC_000010.9:g.69661200T>C NCBI36
NG_031934.1:g.5677A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.241A>G MANE Select ENSP00000362777.3:p.Thr81Ala
ENST00000373673.4:c.241A>G ENSP00000362777.3:p.Thr81Ala
NM_145178.3:c.241A>G NP_660161.1:p.Thr81Ala
NM_145178.4:c.241A>G MANE Select NP_660161.1:p.Thr81Ala
Search 100 bp 5'
Search 100 bp 3'