Canonical Allele Identifier: CA12740009
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs10088218

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531703G>A , CM000670.2:g.128531703G>A GRCh38
NC_000008.10:g.129543949G>A , CM000670.1:g.129543949G>A GRCh37
NC_000008.9:g.129613131G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29367C>T