Canonical Allele Identifier: CA2355189684
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982731071
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070134_22070135insCT , CM000682.2:g.22070134_22070135insCT GRCh38
NC_000020.10:g.22050772_22050773insCT , CM000682.1:g.22050772_22050773insCT GRCh37
NC_000020.9:g.21998772_21998773insCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1446_445+1447insCT
Search 100 bp 5'
Search 100 bp 3'