Canonical Allele Identifier: CA314692469
Gene: LINC01734 HGNC NCBI

Linked Data

dbSNP Id: rs6028335

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.39216834A>G , CM000682.2:g.39216834A>G GRCh38
NC_000020.10:g.37845477A>G , CM000682.1:g.37845477A>G GRCh37
NC_000020.9:g.37278891A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027124.1:n.195-722T>C
XR_001754587.1:n.148-2753A>G