Canonical Allele Identifier: CA11121354
Gene: LINC01104 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.100208905C>T
GRCh37 chr2:g.100825367C>T
gnomAD v2:
2:100825367 C / T
gnomAD v3:
2:100208905 C / T
gnomAD v4:
chr2-100208905-C-T
Joint Max Group AF 0.59230027 (EAS)
Genomes Max Group AF 0.59230027 (EAS)
Exomes Max Group AF 0.227719 (NFE)
dbSNP:
9653442
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100208905C>T , CM000664.2:g.100208905C>T GRCh38
NC_000002.11:g.100825367C>T , CM000664.1:g.100825367C>T GRCh37
NC_000002.10:g.100191799C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+85C>T
Search 100 bp 5'
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