Canonical Allele Identifier: CA270150944
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1042682589
MyVariant Identifiers: chr15:g.45544028A>G (hg19) chr15:g.45251830A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251830A>G , CM000677.2:g.45251830A>G GRCh38
NC_000015.9:g.45544028A>G , CM000677.1:g.45544028A>G GRCh37
NC_000015.8:g.43331320A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.423T>C
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