Canonical Allele Identifier: CA209187827
Gene: DDX50 HGNC NCBI

Linked Data

dbSNP Id: rs916426816
gnomAD v2: 10-70712070-C-T
gnomAD v3: 10-68952314-C-T
gnomAD v4: 10-68952314-C-T
MyVariant Identifiers: chr10:g.70712070C>T (hg19) chr10:g.68952314C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68952314C>T , CM000672.2:g.68952314C>T GRCh38
NC_000010.10:g.70712070C>T , CM000672.1:g.70712070C>T GRCh37
NC_000010.9:g.70382076C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017016626.1:c.*1539-3444C>T XP_016872115.1:n.*1539-3444C>T
Search 100 bp 5'
Search 100 bp 3'