Canonical Allele Identifier: CA13648521
Gene: LINC01465 HGNC NCBI

Linked Data

dbSNP Id: rs10877887

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603400T>C , CM000674.2:g.62603400T>C GRCh38
NC_000012.11:g.62997180T>C , CM000674.1:g.62997180T>C GRCh37
NC_000012.10:g.61283447T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.35A>G