Canonical Allele Identifier: CA855900366
Gene: LINC02235 HGNC NCBI

Linked Data

dbSNP Id: rs1235661582
gnomAD v3: 8-81859830-A-C
gnomAD v4: 8-81859830-A-C
MyVariant Identifiers: chr8:g.82772065A>C (hg19) chr8:g.81859830A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81859830A>C , CM000670.2:g.81859830A>C GRCh38
NC_000008.10:g.82772065A>C , CM000670.1:g.82772065A>C GRCh37
NC_000008.9:g.82934620A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170313.1:n.54-13572A>C
NR_170314.1:n.223+10723A>C
NR_170315.1:n.273-13572A>C
NR_170316.1:n.360+5994A>C
NR_170317.1:n.481+5994A>C
NR_170318.1:n.755+5994A>C
NR_170319.1:n.54-3579A>C
NR_170320.1:n.616-3579A>C
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