Canonical Allele Identifier: CA270151054
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1005306380

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251929G>T , CM000677.2:g.45251929G>T GRCh38
NC_000015.9:g.45544127G>T , CM000677.1:g.45544127G>T GRCh37
NC_000015.8:g.43331419G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.324C>A