ClinGen Allele Registry
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Canonical Allele Identifier:
CA243588916
Gene: LINC02356
HGNC
NCBI
Linked Data
dbSNP Id:
rs149212747
gnomAD v2:
12-111836771-A-AC
gnomAD v3:
12-111398967-A-AC
gnomAD v4:
12-111398967-A-AC
MyVariant Identifiers:
chr12:g.111836772_111836773insC (hg19)
chr12:g.111836771_111836772insC (hg19)
chr12:g.111398968_111398969insC (hg38)
chr12:g.111398967_111398968insC (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.111398974dup , CM000674.2:g.111398974dup
GRCh38
NC_000012.11:g.111836778dup , CM000674.1:g.111836778dup
GRCh37
NC_000012.10:g.110321161dup
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_945342.1:n.44+2101dup
Search 100 bp 5'
Search 100 bp 3'