ClinGen Allele Registry
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Canonical Allele Identifier:
CA274415614
Gene: LINC02883
HGNC
NCBI
Linked Data
dbSNP Id:
rs1012974321
gnomAD v3:
15-85756936-A-C
gnomAD v4:
15-85756936-A-C
MyVariant Identifiers:
chr15:g.86300167A>C (hg19)
chr15:g.85756936A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.85756936A>C , CM000677.2:g.85756936A>C
GRCh38
NC_000015.9:g.86300167A>C , CM000677.1:g.86300167A>C
GRCh37
NC_000015.8:g.84101171A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120366.1:n.419+948T>G
Search 100 bp 5'
Search 100 bp 3'