Canonical Allele Identifier: CA209187831
Gene: DDX50 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
XM_017016626.1:c.*1539-3422G>C XP_016872115.1:n.*1539-3422G>C
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