Canonical Allele Identifier: CA16044463
Gene: LINC01409 HGNC NCBI

Linked Data

dbSNP Id: rs12564807
gnomAD v2: 1-734462-G-A
gnomAD v3: 1-799082-G-A
gnomAD v4: 1-799082-G-A

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