Canonical Allele Identifier: CA185874427
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs912008707

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531644A>G , CM000670.2:g.128531644A>G GRCh38
NC_000008.10:g.129543890A>G , CM000670.1:g.129543890A>G GRCh37
NC_000008.9:g.129613072A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29426T>C