Canonical Allele Identifier: CA2070491664
Gene: LINC02405 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_104646.1:n.1114+2850C=