Canonical Allele Identifier: CA10778632
Gene: LINC01768 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.109896858C>T
GRCh37 chr1:g.110439480C>T
gnomAD v2:
1:110439480 C / T
gnomAD v3:
1:109896858 C / T
gnomAD v4:
chr1-109896858-C-T
Joint Max Group AF 0.95604885 (EAS)
Genomes Max Group AF 0.95604885 (EAS)
Exomes Max Group AF 0.46952186 (NFE)
dbSNP:
333960
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109896858C>T , CM000663.2:g.109896858C>T GRCh38
NC_000001.10:g.110439480C>T , CM000663.1:g.110439480C>T GRCh37
NC_000001.9:g.110241003C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738180.2:n.846-8849C>T
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