Canonical Allele Identifier: CA1839594734
Gene: LINC01239 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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