Canonical Allele Identifier: CA1119101198
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs957656612
gnomAD v3: 8-128547213-C-G
gnomAD v4: 8-128547213-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547213C>G , CM000670.2:g.128547213C>G GRCh38
NC_000008.10:g.129559459C>G , CM000670.1:g.129559459C>G GRCh37
NC_000008.9:g.129628641C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13857G>C
Search 100 bp 5'
Search 100 bp 3'