Canonical Allele Identifier: CA2035362839
Gene: LINC02395 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49925303A= , CM000674.2:g.49925303A= GRCh38
NC_000012.11:g.50319086A= , CM000674.1:g.50319086A= GRCh37
NC_000012.10:g.48605353A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110048.1:n.2813A=