Canonical Allele Identifier: CA79017911
Gene: LINC00506 HGNC NCBI
COSMIC:
COSN17132737 (not active)
COSN17139024 (not active)
COSN17151052 (not active)
MyVariant.info:
GRCh38 chr3:g.87103019A>G
GRCh37 chr3:g.87152169A>G
gnomAD v2:
3:87152169 A / G
gnomAD v3:
3:87103019 A / G
gnomAD v4:
chr3-87103019-A-G
Joint Max Group AF 0.41052887 (AFR)
Genomes Max Group AF 0.41052887 (AFR)
dbSNP:
9284813
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87103019A>G , CM000665.2:g.87103019A>G GRCh38
NC_000003.11:g.87152169A>G , CM000665.1:g.87152169A>G GRCh37
NC_000003.10:g.87234859A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.328+13412A>G
Search 100 bp 5'
Search 100 bp 3'