ClinGen Allele Registry
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Canonical Allele Identifier:
CA79020299
Gene: LINC00506
HGNC
NCBI
Linked Data
dbSNP Id:
rs560091030
gnomAD v2:
3-87173183-A-G
gnomAD v3:
3-87124033-A-G
gnomAD v4:
3-87124033-A-G
MyVariant Identifiers:
chr3:g.87173183A>G (hg19)
chr3:g.87124033A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.87124033A>G , CM000665.2:g.87124033A>G
GRCh38
NC_000003.11:g.87173183A>G , CM000665.1:g.87173183A>G
GRCh37
NC_000003.10:g.87255873A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104153.1:n.329-30305A>G
Search 100 bp 5'
Search 100 bp 3'