Canonical Allele Identifier: CA490222272
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1206082370
gnomAD v4: 15-45251697-C-A
MyVariant Identifiers: chr15:g.45543895C>A (hg19) chr15:g.45251697C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251697C>A , CM000677.2:g.45251697C>A GRCh38
NC_000015.9:g.45543895C>A , CM000677.1:g.45543895C>A GRCh37
NC_000015.8:g.43331187C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.556G>T
Search 100 bp 5'
Search 100 bp 3'