ClinGen Allele Registry
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Canonical Allele Identifier:
CA79020306
Gene: LINC00506
HGNC
NCBI
Linked Data
dbSNP Id:
rs770772093
gnomAD v2:
3-87173248-T-C
gnomAD v3:
3-87124098-T-C
gnomAD v4:
3-87124098-T-C
MyVariant Identifiers:
chr3:g.87173248T>C (hg19)
chr3:g.87124098T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.87124098T>C , CM000665.2:g.87124098T>C
GRCh38
NC_000003.11:g.87173248T>C , CM000665.1:g.87173248T>C
GRCh37
NC_000003.10:g.87255938T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104153.1:n.329-30240T>C
Search 100 bp 5'
Search 100 bp 3'