Canonical Allele Identifier: CA14078867
Gene: SLC28A2-AS1 HGNC NCBI
SLC28A2 HGNC NCBI
COSMIC:
COSN6544262 (not active)
MyVariant.info:
GRCh38 chr15:g.45252090T>A
GRCh37 chr15:g.45544288T>A
gnomAD v2:
15:45544288 T / A
gnomAD v3:
15:45252090 T / A
gnomAD v4:
chr15-45252090-T-A
Joint Max Group AF 0.68150948 (NFE)
Genomes Max Group AF 0.67941944 (NFE)
Exomes Max Group AF 0.68081839 (NFE)
dbSNP:
2413775
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45252090T>A , CM000677.2:g.45252090T>A GRCh38
NC_000015.9:g.45544288T>A , CM000677.1:g.45544288T>A GRCh37
NC_000015.8:g.43331580T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.181-18A>T (SLC28A2-AS1)
XM_011522198.1:c.-230T>A (SLC28A2) XP_011520500.1:n.-230T>A
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