Canonical Allele Identifier: CA490223529
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1482184570
gnomAD v2: 15-45544082-C-G
gnomAD v3: 15-45251884-C-G
gnomAD v4: 15-45251884-C-G
MyVariant Identifiers: chr15:g.45544082C>G (hg19) chr15:g.45251884C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251884C>G , CM000677.2:g.45251884C>G GRCh38
NC_000015.9:g.45544082C>G , CM000677.1:g.45544082C>G GRCh37
NC_000015.8:g.43331374C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.369G>C
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