Canonical Allele Identifier: CA969335414
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899796002
gnomAD v3: 15-45251764-C-CTTTTG
gnomAD v4: 15-45251764-C-CTTTTG
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251779_45251783dup , CM000677.2:g.45251779_45251783dup GRCh38
NC_000015.9:g.45543977_45543981dup , CM000677.1:g.45543977_45543981dup GRCh37
NC_000015.8:g.43331269_43331273dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.484_488dup
Search 100 bp 5'
Search 100 bp 3'