Canonical Allele Identifier: CA480537642
Gene: LINC01465 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.62997089T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603309T>G , CM000674.2:g.62603309T>G GRCh38
NC_000012.11:g.62997089T>G , CM000674.1:g.62997089T>G GRCh37
NC_000012.10:g.61283356T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.126A>C