Canonical Allele Identifier: CA68900705
Gene: LINC01266 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.842168G>A
GRCh37 chr3:g.883851G>A
gnomAD v2:
3:883851 G / A
gnomAD v3:
3:842168 G / A
gnomAD v4:
chr3-842168-G-A
Joint Max Group AF 0.6317392 (NFE)
Genomes Max Group AF 0.6317392 (NFE)
dbSNP:
4684585
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.842168G>A , CM000665.2:g.842168G>A GRCh38
NC_000003.11:g.883851G>A , CM000665.1:g.883851G>A GRCh37
NC_000003.10:g.858851G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110118.1:n.212-208G>A
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