Canonical Allele Identifier: CA490222544
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1312583563
gnomAD v2: 15-45543942-T-C
gnomAD v3: 15-45251744-T-C
gnomAD v4: 15-45251744-T-C
MyVariant Identifiers: chr15:g.45543942T>C (hg19) chr15:g.45251744T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251744T>C , CM000677.2:g.45251744T>C GRCh38
NC_000015.9:g.45543942T>C , CM000677.1:g.45543942T>C GRCh37
NC_000015.8:g.43331234T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.509A>G
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