Canonical Allele Identifier: CA2041301929
Gene: LINC01465 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603402C= , CM000674.2:g.62603402C= GRCh38
NC_000012.11:g.62997182C= , CM000674.1:g.62997182C= GRCh37
NC_000012.10:g.61283449C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.33G=