Canonical Allele Identifier: CA1016142146
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070110-C-CTTT
gnomAD v4: 20-22070110-C-CTTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070112_22070113insTTT , CM000682.2:g.22070112_22070113insTTT GRCh38
NC_000020.10:g.22050750_22050751insTTT , CM000682.1:g.22050750_22050751insTTT GRCh37
NC_000020.9:g.21998750_21998751insTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1424_445+1425insTTT
Search 100 bp 5'
Search 100 bp 3'