ClinGen Allele Registry
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Canonical Allele Identifier:
CA544782027
Gene: LINC00506
HGNC
NCBI
Linked Data
dbSNP Id:
rs1267036831
gnomAD v2:
3-87173323-C-T
gnomAD v3:
3-87124173-C-T
gnomAD v4:
3-87124173-C-T
MyVariant Identifiers:
chr3:g.87173323C>T (hg19)
chr3:g.87124173C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.87124173C>T , CM000665.2:g.87124173C>T
GRCh38
NC_000003.11:g.87173323C>T , CM000665.1:g.87173323C>T
GRCh37
NC_000003.10:g.87256013C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104153.1:n.329-30165C>T
Search 100 bp 5'
Search 100 bp 3'