Canonical Allele Identifier: CA1839594735
Gene: LINC01239 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22770887A>T , CM000671.2:g.22770887A>T GRCh38
NC_000009.11:g.22770886A>T , CM000671.1:g.22770886A>T GRCh37
NC_000009.10:g.22760886A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038977.1:n.524+47457A>T