ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA274415639
Gene: LINC02883
HGNC
NCBI
Linked Data
dbSNP Id:
rs1031910435
gnomAD v3:
15-85756980-G-A
gnomAD v4:
15-85756980-G-A
MyVariant Identifiers:
chr15:g.86300211G>A (hg19)
chr15:g.85756980G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.85756980G>A , CM000677.2:g.85756980G>A
GRCh38
NC_000015.9:g.86300211G>A , CM000677.1:g.86300211G>A
GRCh37
NC_000015.8:g.84101215G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_120366.1:n.419+904C>T
Search 100 bp 5'
Search 100 bp 3'