Canonical Allele Identifier: CA2348311432
Gene: LINC01428 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.7199409T>G , CM000682.2:g.7199409T>G GRCh38
NC_000020.10:g.7180056T>G , CM000682.1:g.7180056T>G GRCh37
NC_000020.9:g.7128056T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110609.1:n.165-10842A>C