Canonical Allele Identifier: CA13753262
Gene: LINC02398 HGNC NCBI

Linked Data

dbSNP Id: rs11045000
gnomAD v2: 12-20184146-G-A
gnomAD v3: 12-20031212-G-A
gnomAD v4: 12-20031212-G-A
MyVariant Identifiers: chr12:g.20184146G>A (hg19) chr12:g.20031212G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20031212G>A , CM000674.2:g.20031212G>A GRCh38
NC_000012.11:g.20184146G>A , CM000674.1:g.20184146G>A GRCh37
NC_000012.10:g.20075413G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040098.1:n.409+11516G>A
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