Canonical Allele Identifier: CA2174010029
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251778_45251779delinsTG , CM000677.2:g.45251778_45251779delinsTG GRCh38
NC_000015.9:g.45543976_45543977delinsTG , CM000677.1:g.45543976_45543977delinsTG GRCh37
NC_000015.8:g.43331268_43331269delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.474_475delinsCA