Canonical Allele Identifier: CA490222650
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45543958A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251760A>T , CM000677.2:g.45251760A>T GRCh38
NC_000015.9:g.45543958A>T , CM000677.1:g.45543958A>T GRCh37
NC_000015.8:g.43331250A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.493T>A
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