Canonical Allele Identifier: CA660460967
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1337117787
gnomAD v3: 10-117524779-C-T
gnomAD v4: 10-117524779-C-T
MyVariant Identifiers: chr10:g.119284290C>T (hg19) chr10:g.117524779C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524779C>T , CM000672.2:g.117524779C>T GRCh38
NC_000010.10:g.119284290C>T , CM000672.1:g.119284290C>T GRCh37
NC_000010.9:g.119274280C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19527G>A
NR_144378.1:n.493+17318G>A
Search 100 bp 5'
Search 100 bp 3'