Canonical Allele Identifier: CA667865382
Gene: DDX50 HGNC NCBI

Linked Data

dbSNP Id: rs1281032304
gnomAD v3: 10-68952329-G-A
gnomAD v4: 10-68952329-G-A
MyVariant Identifiers: chr10:g.70712085G>A (hg19) chr10:g.68952329G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68952329G>A , CM000672.2:g.68952329G>A GRCh38
NC_000010.10:g.70712085G>A , CM000672.1:g.70712085G>A GRCh37
NC_000010.9:g.70382091G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017016626.1:c.*1539-3429G>A XP_016872115.1:n.*1539-3429G>A
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