Canonical Allele Identifier: CA215023059
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs945259201
gnomAD v2: 10-119284303-G-T
gnomAD v3: 10-117524792-G-T
gnomAD v4: 10-117524792-G-T
MyVariant Identifiers: chr10:g.119284303G>T (hg19) chr10:g.117524792G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524792G>T , CM000672.2:g.117524792G>T GRCh38
NC_000010.10:g.119284303G>T , CM000672.1:g.119284303G>T GRCh37
NC_000010.9:g.119274293G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19514C>A
NR_144378.1:n.493+17305C>A
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