Canonical Allele Identifier: CA313072785
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs374017808
gnomAD v2: 20-22050750-TC-T
gnomAD v3: 20-22070112-TC-T
gnomAD v4: 20-22070112-TC-T
MyVariant Identifiers: chr20:g.22050751del (hg19) chr20:g.22070113del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070113del , CM000682.2:g.22070113del GRCh38
NC_000020.10:g.22050751del , CM000682.1:g.22050751del GRCh37
NC_000020.9:g.21998751del NCBI36

Transcript Alleles

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