Canonical Allele Identifier: CA660460944
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs964065246
gnomAD v3: 10-117524766-G-C
gnomAD v4: 10-117524766-G-C
MyVariant Identifiers: chr10:g.119284277G>C (hg19) chr10:g.117524766G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524766G>C , CM000672.2:g.117524766G>C GRCh38
NC_000010.10:g.119284277G>C , CM000672.1:g.119284277G>C GRCh37
NC_000010.9:g.119274267G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19540C>G
NR_144378.1:n.493+17331C>G
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