Canonical Allele Identifier: CA2355184580
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982463920

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059187_22059188del , CM000682.2:g.22059187_22059188del GRCh38
NC_000020.10:g.22039825_22039826del , CM000682.1:g.22039825_22039826del GRCh37
NC_000020.9:g.21987825_21987826del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+4903_195+4904del