Canonical Allele Identifier: CA490223120
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899797092
gnomAD v4: 15-45251826-C-T
MyVariant Identifiers: chr15:g.45544024C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251826C>T , CM000677.2:g.45251826C>T GRCh38
NC_000015.9:g.45544024C>T , CM000677.1:g.45544024C>T GRCh37
NC_000015.8:g.43331316C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.427G>A
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