Canonical Allele Identifier: CA1818921300
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816089682
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529993C>T , CM000670.2:g.128529993C>T GRCh38
NC_000008.10:g.129542239C>T , CM000670.1:g.129542239C>T GRCh37
NC_000008.9:g.129611421C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31077G>A
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