Canonical Allele Identifier: CA2619583769
Gene: LINC01465 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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