Canonical Allele Identifier: CA2041301932
Gene: LINC01465 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603405A= , CM000674.2:g.62603405A= GRCh38
NC_000012.11:g.62997185A= , CM000674.1:g.62997185A= GRCh37
NC_000012.10:g.61283452A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.30T=