ClinGen Allele Registry
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Canonical Allele Identifier:
CA274415601
Gene: LINC02883
HGNC
NCBI
Linked Data
dbSNP Id:
rs1044512657
gnomAD v2:
15-86300144-T-C
gnomAD v3:
15-85756913-T-C
gnomAD v4:
15-85756913-T-C
MyVariant Identifiers:
chr15:g.86300144T>C (hg19)
chr15:g.85756913T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.85756913T>C , CM000677.2:g.85756913T>C
GRCh38
NC_000015.9:g.86300144T>C , CM000677.1:g.86300144T>C
GRCh37
NC_000015.8:g.84101148T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120366.1:n.420-957A>G
Search 100 bp 5'
Search 100 bp 3'