Canonical Allele Identifier: CA2174010031
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899796124

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.474del