ClinGen Allele Registry
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Canonical Allele Identifier:
CA951840610
Gene: LINC02356
HGNC
NCBI
Linked Data
dbSNP Id:
rs1869951101
gnomAD v3:
12-111398959-T-G
gnomAD v4:
12-111398959-T-G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.111398959T>G , CM000674.2:g.111398959T>G
GRCh38
NC_000012.11:g.111836763T>G , CM000674.1:g.111836763T>G
GRCh37
NC_000012.10:g.110321146T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_945342.1:n.44+2086T>G
Search 100 bp 5'
Search 100 bp 3'