Canonical Allele Identifier: CA270150958
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1011436597
gnomAD v3: 15-45251877-C-T
gnomAD v4: 15-45251877-C-T
MyVariant Identifiers: chr15:g.45544075C>T (hg19) chr15:g.45251877C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251877C>T , CM000677.2:g.45251877C>T GRCh38
NC_000015.9:g.45544075C>T , CM000677.1:g.45544075C>T GRCh37
NC_000015.8:g.43331367C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.376G>A
Search 100 bp 5'
Search 100 bp 3'