Canonical Allele Identifier: CA293661345
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69806211A>G , CM000679.2:g.69806211A>G GRCh38
NC_000017.10:g.67802352A>G , CM000679.1:g.67802352A>G GRCh37
NC_000017.9:g.65313947A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.317-39229A>G
NR_109972.1:n.317-39229A>G