Canonical Allele Identifier: CA2355189672
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982730634
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070118_22070119insCTTTTTTTT , CM000682.2:g.22070118_22070119insCTTTTTTTT GRCh38
NC_000020.10:g.22050756_22050757insCTTTTTTTT , CM000682.1:g.22050756_22050757insCTTTTTTTT GRCh37
NC_000020.9:g.21998756_21998757insCTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1430_445+1431insCTTTTTTTT
Search 100 bp 5'
Search 100 bp 3'