Canonical Allele Identifier: CA480537620

Gene: LINC01465

Linked Data

• MyVariant Identifiers: chr12:g.62997084A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.62603304A>T , CM000674.2:g.62603304A>T	GRCh38
NC_000012.11:g.62997084A>T , CM000674.1:g.62997084A>T	GRCh37
NC_000012.10:g.61283351A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121682.1:n.131T>A