Canonical Allele Identifier: CA490222891
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

gnomAD v4: 15-45251799-T-A
MyVariant Identifiers: chr15:g.45543997T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251799T>A , CM000677.2:g.45251799T>A GRCh38
NC_000015.9:g.45543997T>A , CM000677.1:g.45543997T>A GRCh37
NC_000015.8:g.43331289T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.454A>T
Search 100 bp 5'
Search 100 bp 3'