Canonical Allele Identifier: CA209187830
Gene: DDX50 HGNC NCBI

Linked Data

dbSNP Id: rs141366172
gnomAD v2: 10-70712092-G-A
gnomAD v3: 10-68952336-G-A
gnomAD v4: 10-68952336-G-A
MyVariant Identifiers: chr10:g.70712092G>A (hg19) chr10:g.68952336G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68952336G>A , CM000672.2:g.68952336G>A GRCh38
NC_000010.10:g.70712092G>A , CM000672.1:g.70712092G>A GRCh37
NC_000010.9:g.70382098G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017016626.1:c.*1539-3422G>A XP_016872115.1:n.*1539-3422G>A
Search 100 bp 5'
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