Canonical Allele Identifier: CA113945528
Gene: LINC02226 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.8438418C>T
GRCh37 chr5:g.8438531C>T
gnomAD v2:
5:8438531 C / T
gnomAD v3:
5:8438418 C / T
gnomAD v4:
chr5-8438418-C-T
Joint Max Group AF 0.90871961 (EAS)
Genomes Max Group AF 0.90871961 (EAS)
dbSNP:
340669
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8438418C>T , CM000667.2:g.8438418C>T GRCh38
NC_000005.9:g.8438531C>T , CM000667.1:g.8438531C>T GRCh37
NC_000005.8:g.8491531C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+13805G>A
Search 100 bp 5'
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