Canonical Allele Identifier: CA13690657
Gene: LINC02444 HGNC NCBI
MyVariant.info:
GRCh38 chr12:g.73207352C>T
GRCh37 chr12:g.73601132C>T
gnomAD v2:
12:73601132 C / T
gnomAD v3:
12:73207352 C / T
gnomAD v4:
chr12-73207352-C-T
Joint Max Group AF 0.2591592 (NFE)
Genomes Max Group AF 0.25912443 (NFE)
Exomes Max Group AF 0.18664316 (NFE)
dbSNP:
11615274
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.73207352C>T , CM000674.2:g.73207352C>T GRCh38
NC_000012.11:g.73601132C>T , CM000674.1:g.73601132C>T GRCh37
NC_000012.10:g.71887399C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110130.1:n.386-95C>T
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