Canonical Allele Identifier: CA469826834
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991090G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231333G>A , CM000672.2:g.68231333G>A GRCh38
NC_000010.10:g.69991090G>A , CM000672.1:g.69991090G>A GRCh37
NC_000010.9:g.69661096G>A NCBI36
NG_031934.1:g.5781C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.345C>T MANE Select ENSP00000362777.3:p.His115=
ENST00000373673.4:c.345C>T ENSP00000362777.3:p.His115=
NM_145178.3:c.345C>T NP_660161.1:p.His115=
NM_145178.4:c.345C>T MANE Select NP_660161.1:p.His115=