Canonical Allele Identifier: CA48805969
Gene: LINC01122 HGNC NCBI

Linked Data

dbSNP Id: rs372795036
gnomAD v2: 2-59036860-C-T
gnomAD v3: 2-58809725-C-T
gnomAD v4: 2-58809725-C-T
MyVariant Identifiers: chr2:g.59036860C>T (hg19) chr2:g.58809725C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58809725C>T , CM000664.2:g.58809725C>T GRCh38
NC_000002.11:g.59036860C>T , CM000664.1:g.59036860C>T GRCh37
NC_000002.10:g.58890364C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.248-40705C>T
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