Canonical Allele Identifier: CA490222227
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45543886T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251688T>G , CM000677.2:g.45251688T>G GRCh38
NC_000015.9:g.45543886T>G , CM000677.1:g.45543886T>G GRCh37
NC_000015.8:g.43331178T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.565A>C
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