Canonical Allele Identifier: CA490222289
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899794571
gnomAD v3: 15-45251700-A-C
gnomAD v4: 15-45251700-A-C
MyVariant Identifiers: chr15:g.45543898A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251700A>C , CM000677.2:g.45251700A>C GRCh38
NC_000015.9:g.45543898A>C , CM000677.1:g.45543898A>C GRCh37
NC_000015.8:g.43331190A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.553T>G
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