Canonical Allele Identifier: CA931728213
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1351766839

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527929_99527941dup , CM000672.2:g.99527929_99527941dup GRCh38
NC_000010.10:g.101287686_101287698dup , CM000672.1:g.101287686_101287698dup GRCh37
NC_000010.9:g.101277676_101277688dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.454_466dup