ClinGen Allele Registry
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Canonical Allele Identifier:
CA547127617
Gene: LINC02045
HGNC
NCBI
Linked Data
dbSNP Id:
rs1211775460
gnomAD v2:
3-147935597-C-T
MyVariant Identifiers:
chr3:g.147935597C>T (hg19)
chr3:g.148217810C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148217810C>T , CM000665.2:g.148217810C>T
GRCh38
NC_000003.11:g.147935597C>T , CM000665.1:g.147935597C>T
GRCh37
NC_000003.10:g.149418287C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_924565.1:n.86+2700G>A
Search 100 bp 5'
Search 100 bp 3'