Canonical Allele Identifier: CA653292691
Gene: LNCAROD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52464156G>T , CM000672.2:g.52464156G>T GRCh38
NC_000010.10:g.54223916G>T , CM000672.1:g.54223916G>T GRCh37
NC_000010.9:g.53893922G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120641.1:n.138-824C>A