ClinGen Allele Registry
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Canonical Allele Identifier:
CA15842826
Gene: LINC02883
HGNC
NCBI
Linked Data
dbSNP Id:
rs62025270
gnomAD v2:
15-86300198-G-A
gnomAD v3:
15-85756967-G-A
gnomAD v4:
15-85756967-G-A
MyVariant Identifiers:
chr15:g.86300198G>A (hg19)
chr15:g.85756967G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.85756967G>A , CM000677.2:g.85756967G>A
GRCh38
NC_000015.9:g.86300198G>A , CM000677.1:g.86300198G>A
GRCh37
NC_000015.8:g.84101202G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_120366.1:n.419+917C>T
Search 100 bp 5'
Search 100 bp 3'