Canonical Allele Identifier: CA1493651071
Gene: LINC02465 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.129810129T= , CM000666.2:g.129810129T= GRCh38
NC_000004.11:g.130731284T= , CM000666.1:g.130731284T= GRCh37
NC_000004.10:g.130950734T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_151713.1:n.429-1873T=