Canonical Allele Identifier: CA2174010253
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45252000G= , CM000677.2:g.45252000G= GRCh38
NC_000015.9:g.45544198G= , CM000677.1:g.45544198G= GRCh37
NC_000015.8:g.43331490G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120335.1:n.253C=