Canonical Allele Identifier: CA215023071
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs995609105
gnomAD v2: 10-119284406-T-A
gnomAD v3: 10-117524895-T-A
gnomAD v4: 10-117524895-T-A
MyVariant Identifiers: chr10:g.119284406T>A (hg19) chr10:g.117524895T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524895T>A , CM000672.2:g.117524895T>A GRCh38
NC_000010.10:g.119284406T>A , CM000672.1:g.119284406T>A GRCh37
NC_000010.9:g.119274396T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19411A>T
NR_144378.1:n.493+17202A>T
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