Canonical Allele Identifier: CA2815543177
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070112_22070113insTTTTT , CM000682.2:g.22070112_22070113insTTTTT GRCh38
NC_000020.10:g.22050750_22050751insTTTTT , CM000682.1:g.22050750_22050751insTTTTT GRCh37
NC_000020.9:g.21998750_21998751insTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1424_445+1425insTTTTT