Canonical Allele Identifier: CA480537659
Gene: LINC01465 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.62997093T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603313T>A , CM000674.2:g.62603313T>A GRCh38
NC_000012.11:g.62997093T>A , CM000674.1:g.62997093T>A GRCh37
NC_000012.10:g.61283360T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.122A>T
Search 100 bp 5'
Search 100 bp 3'