Canonical Allele Identifier: CA2560537639
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854761T>G , CM000679.2:g.69854761T>G GRCh38
NC_000017.10:g.67850902T>G , CM000679.1:g.67850902T>G GRCh37
NC_000017.9:g.65362497T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9275T>G
NR_109972.1:n.363+9275T>G