Canonical Allele Identifier: CA2020449101
Gene: LINC02398 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20077705A= , CM000674.2:g.20077705A= GRCh38
NC_000012.11:g.20230639A= , CM000674.1:g.20230639A= GRCh37
NC_000012.10:g.20121906A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040098.1:n.410-21047A=