Canonical Allele Identifier: CA635117102
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1555784632
gnomAD v2: 20-22050748-C-CTTTTTTTTTTTT
MyVariant Identifiers: chr20:g.22050748_22050749insTTTTTTTTTTTT (hg19) chr20:g.22070110_22070111insTTTTTTTTTTTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070112_22070113insTTTTTTTTTTTT , CM000682.2:g.22070112_22070113insTTTTTTTTTTTT GRCh38
NC_000020.10:g.22050750_22050751insTTTTTTTTTTTT , CM000682.1:g.22050750_22050751insTTTTTTTTTTTT GRCh37
NC_000020.9:g.21998750_21998751insTTTTTTTTTTTT NCBI36

Transcript Alleles

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