Canonical Allele Identifier: CA667865351
Gene: DDX50 HGNC NCBI

Linked Data

dbSNP Id: rs1248470488
gnomAD v3: 10-68952309-CAT-C
gnomAD v4: 10-68952309-CAT-C
MyVariant Identifiers: chr10:g.70712066_70712067del (hg19) chr10:g.68952310_68952311del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68952310_68952311del , CM000672.2:g.68952310_68952311del GRCh38
NC_000010.10:g.70712066_70712067del , CM000672.1:g.70712066_70712067del GRCh37
NC_000010.9:g.70382072_70382073del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017016626.1:c.*1539-3448_*1539-3447del XP_016872115.1:n.*1539-3448_*1539-3447del...
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