Canonical Allele Identifier: CA1016142463
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982731424

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070137del , CM000682.2:g.22070137del GRCh38
NC_000020.10:g.22050775del , CM000682.1:g.22050775del GRCh37
NC_000020.9:g.21998775del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1449del