Canonical Allele Identifier: CA2619583778
Gene: LINC01465 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603406G>T , CM000674.2:g.62603406G>T GRCh38
NC_000012.11:g.62997186G>T , CM000674.1:g.62997186G>T GRCh37
NC_000012.10:g.61283453G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.29C>A