ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA243588766
Gene: LINC02356
HGNC
NCBI
Linked Data
dbSNP Id:
rs1039383298
gnomAD v3:
12-111398808-C-T
gnomAD v4:
12-111398808-C-T
MyVariant Identifiers:
chr12:g.111836612C>T (hg19)
chr12:g.111398808C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.111398808C>T , CM000674.2:g.111398808C>T
GRCh38
NC_000012.11:g.111836612C>T , CM000674.1:g.111836612C>T
GRCh37
NC_000012.10:g.110320995C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_945342.1:n.44+1935C>T
Search 100 bp 5'
Search 100 bp 3'