Canonical Allele Identifier: CA1119101202
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816381174
gnomAD v3: 8-128547275-T-C
gnomAD v4: 8-128547275-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547275T>C , CM000670.2:g.128547275T>C GRCh38
NC_000008.10:g.129559521T>C , CM000670.1:g.129559521T>C GRCh37
NC_000008.9:g.129628703T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13795A>G
Search 100 bp 5'
Search 100 bp 3'