Canonical Allele Identifier: CA11261727
Gene: LINC01090 HGNC NCBI
dbSNP:
7582658
gnomAD v2:
2:188947841 A / G
gnomAD v3:
2:188083114 A / G
gnomAD v4:
chr2-188083114-A-G
Joint Max Group AF 0.59500862 (EAS)
Genomes Max Group AF 0.59500862 (EAS)
MyVariant.info:
GRCh38 chr2:g.188083114A>G
GRCh37 chr2:g.188947841A>G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188083114A>G , CM000664.2:g.188083114A>G GRCh38
NC_000002.11:g.188947841A>G , CM000664.1:g.188947841A>G GRCh37
NC_000002.10:g.188656086A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126396.1:n.381-47403T>C
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