Canonical Allele Identifier: CA2355189582
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982726150

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069951del , CM000682.2:g.22069951del GRCh38
NC_000020.10:g.22050589del , CM000682.1:g.22050589del GRCh37
NC_000020.9:g.21998589del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1263del