Canonical Allele Identifier: CA28721986
Gene: LINC01397 HGNC NCBI

Linked Data

dbSNP Id: rs17025426

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110102705C>T , CM000663.2:g.110102705C>T GRCh38
NC_000001.10:g.110645327C>T , CM000663.1:g.110645327C>T GRCh37
NC_000001.9:g.110446850C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126382.1:n.166-6140C>T