Canonical Allele Identifier: CA932986913
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1846312908
gnomAD v3: 10-117524994-A-G
gnomAD v4: 10-117524994-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524994A>G , CM000672.2:g.117524994A>G GRCh38
NC_000010.10:g.119284505A>G , CM000672.1:g.119284505A>G GRCh37
NC_000010.9:g.119274495A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002791.2:n.574+19312T>C
NR_144378.1:n.493+17103T>C
Search 100 bp 5'
Search 100 bp 3'