Canonical Allele Identifier: CA1016157207
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982461905
gnomAD v3: 20-22059132-C-A
gnomAD v4: 20-22059132-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059132C>A , CM000682.2:g.22059132C>A GRCh38
NC_000020.10:g.22039770C>A , CM000682.1:g.22039770C>A GRCh37
NC_000020.9:g.21987770C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+4848C>A
Search 100 bp 5'
Search 100 bp 3'