Canonical Allele Identifier: CA2272849667
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854669A= , CM000679.2:g.69854669A= GRCh38
NC_000017.10:g.67850810A= , CM000679.1:g.67850810A= GRCh37
NC_000017.9:g.65362405A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9183A=
NR_109972.1:n.363+9183A=