Canonical Allele Identifier: CA2355189667
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070111_22070113delinsTTC , CM000682.2:g.22070111_22070113delinsTTC GRCh38
NC_000020.10:g.22050749_22050751delinsTTC , CM000682.1:g.22050749_22050751delinsTTC GRCh37
NC_000020.9:g.21998749_21998751delinsTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1423_445+1425delinsTTC