Canonical Allele Identifier: CA635117104
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1555784632
gnomAD v2: 20-22050748-C-CTTTTTTTTTTTTTTTTTTTT
MyVariant Identifiers: chr20:g.22050748_22050749insTTTTTTTTTTTTTTTTTTTT (hg19) chr20:g.22070110_22070111insTTTTTTTTTTTTTTTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070112_22070113insTTTTTTTTTTTTTTTTTTTT , CM000682.2:g.22070112_22070113insTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000020.10:g.22050750_22050751insTTTTTTTTTTTTTTTTTTTT , CM000682.1:g.22050750_22050751insTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000020.9:g.21998750_21998751insTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1424_445+1425insTTTTTTTTTTTTTTTTTTTT
Search 100 bp 5'
Search 100 bp 3'