ClinGen Allele Registry
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Canonical Allele Identifier:
CA490223350
Gene: SLC28A2-AS1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr15:g.45544059G>C (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.45251861G>C , CM000677.2:g.45251861G>C
GRCh38
NC_000015.9:g.45544059G>C , CM000677.1:g.45544059G>C
GRCh37
NC_000015.8:g.43331351G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120335.1:n.392C>G
Search 100 bp 5'
Search 100 bp 3'