Canonical Allele Identifier: CA15419385
Gene: LINC01411 HGNC NCBI

Linked Data

dbSNP Id: rs12659144

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174350517T>C , CM000667.2:g.174350517T>C GRCh38
NC_000005.9:g.173777520T>C , CM000667.1:g.173777520T>C GRCh37
NC_000005.8:g.173710126T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125806.1:n.223+13941T>C