Canonical Allele Identifier: CA270150890
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1041090715
gnomAD v3: 15-45251757-C-A
gnomAD v4: 15-45251757-C-A
MyVariant Identifiers: chr15:g.45543955C>A (hg19) chr15:g.45251757C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251757C>A , CM000677.2:g.45251757C>A GRCh38
NC_000015.9:g.45543955C>A , CM000677.1:g.45543955C>A GRCh37
NC_000015.8:g.43331247C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.496G>T
Search 100 bp 5'
Search 100 bp 3'