Canonical Allele Identifier: CA742128210
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1446864578
gnomAD v3: 20-22069866-AG-A
gnomAD v4: 20-22069866-AG-A
MyVariant Identifiers: chr20:g.22050505del (hg19) chr20:g.22069867del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069867del , CM000682.2:g.22069867del GRCh38
NC_000020.10:g.22050505del , CM000682.1:g.22050505del GRCh37
NC_000020.9:g.21998505del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1179del
Search 100 bp 5'
Search 100 bp 3'