Canonical Allele Identifier: CA16044463
Gene: LINC01409 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.799082G>A
GRCh37 chr1:g.734462G>A
gnomAD v2:
1:734462 G / A
gnomAD v3:
1:799082 G / A
gnomAD v4:
chr1-799082-G-A
Joint Max Group AF 0.93188994 (EAS)
Genomes Max Group AF 0.93188994 (EAS)
dbSNP:
12564807
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.799082G>A , CM000663.2:g.799082G>A GRCh38
NC_000001.10:g.734462G>A , CM000663.1:g.734462G>A GRCh37
NC_000001.9:g.724325G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000634337.2:n.127+28588C>T
ENST00000635509.2:n.100+28588C>T
XR_002958522.1:n.71-4485G>A
XR_002958525.1:n.285-4869G>A
XR_946806.3:n.352-4837G>A
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