Canonical Allele Identifier: CA1818908630
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1239570612
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547074C>G , CM000670.2:g.128547074C>G GRCh38
NC_000008.10:g.129559320C>G , CM000670.1:g.129559320C>G GRCh37
NC_000008.9:g.129628502C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13996G>C
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