Canonical Allele Identifier: CA928410205
Gene: LNCAROD HGNC NCBI

Linked Data

dbSNP Id: rs1837730730

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52464172G>A , CM000672.2:g.52464172G>A GRCh38
NC_000010.10:g.54223932G>A , CM000672.1:g.54223932G>A GRCh37
NC_000010.9:g.53893938G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120641.1:n.138-840C>T