Canonical Allele Identifier: CA2810289086
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854942A>T , CM000679.2:g.69854942A>T GRCh38
NC_000017.10:g.67851083A>T , CM000679.1:g.67851083A>T GRCh37
NC_000017.9:g.65362678A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9456A>T
NR_109972.1:n.363+9456A>T