Canonical Allele Identifier: CA490222339
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1199673472
gnomAD v3: 15-45251709-T-A
gnomAD v4: 15-45251709-T-A
MyVariant Identifiers: chr15:g.45543907T>A (hg19) chr15:g.45251709T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251709T>A , CM000677.2:g.45251709T>A GRCh38
NC_000015.9:g.45543907T>A , CM000677.1:g.45543907T>A GRCh37
NC_000015.8:g.43331199T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.544A>T
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