Canonical Allele Identifier: CA656855458
Gene: LINC01483 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854737A>C , CM000679.2:g.69854737A>C GRCh38
NC_000017.10:g.67850878A>C , CM000679.1:g.67850878A>C GRCh37
NC_000017.9:g.65362473A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9251A>C
NR_109972.1:n.363+9251A>C