Canonical Allele Identifier: CA270150997
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1044699959
gnomAD v4: 15-45251892-G-A
MyVariant Identifiers: chr15:g.45544090G>A (hg19) chr15:g.45251892G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251892G>A , CM000677.2:g.45251892G>A GRCh38
NC_000015.9:g.45544090G>A , CM000677.1:g.45544090G>A GRCh37
NC_000015.8:g.43331382G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.361C>T
Search 100 bp 5'
Search 100 bp 3'