Canonical Allele Identifier: CA12730412
Gene: LINC02235 HGNC NCBI

Linked Data

dbSNP Id: rs67666182
gnomAD v2: 8-82772037-A-G
gnomAD v3: 8-81859802-A-G
gnomAD v4: 8-81859802-A-G
MyVariant Identifiers: chr8:g.82772037A>G (hg19) chr8:g.81859802A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81859802A>G , CM000670.2:g.81859802A>G GRCh38
NC_000008.10:g.82772037A>G , CM000670.1:g.82772037A>G GRCh37
NC_000008.9:g.82934592A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170313.1:n.54-13600A>G
NR_170314.1:n.223+10695A>G
NR_170315.1:n.273-13600A>G
NR_170316.1:n.360+5966A>G
NR_170317.1:n.481+5966A>G
NR_170318.1:n.755+5966A>G
NR_170319.1:n.54-3607A>G
NR_170320.1:n.616-3607A>G
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