Canonical Allele Identifier: CA684971337
Gene: LINC02405 HGNC NCBI

Linked Data

dbSNP Id: rs10773338

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.126919857G>T , CM000674.2:g.126919857G>T GRCh38
NC_000012.11:g.127404403G>T , CM000674.1:g.127404403G>T GRCh37
NC_000012.10:g.125970356G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104646.1:n.1114+2850C>A