Canonical Allele Identifier: CA1016157277
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1256970887
gnomAD v3: 20-22059257-G-T
gnomAD v4: 20-22059257-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059257G>T , CM000682.2:g.22059257G>T GRCh38
NC_000020.10:g.22039895G>T , CM000682.1:g.22039895G>T GRCh37
NC_000020.9:g.21987895G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4973G>T
Search 100 bp 5'
Search 100 bp 3'