Canonical Allele Identifier: CA313072743
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs888542670
gnomAD v2: 20-22050327-G-GA
gnomAD v3: 20-22069689-G-GA
gnomAD v4: 20-22069689-G-GA
MyVariant Identifiers: chr20:g.22050328_22050329insA (hg19) chr20:g.22050327_22050328insA (hg19) chr20:g.22069690_22069691insA (hg38) chr20:g.22069689_22069690insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069697dup , CM000682.2:g.22069697dup GRCh38
NC_000020.10:g.22050335dup , CM000682.1:g.22050335dup GRCh37
NC_000020.9:g.21998335dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1009dup
Search 100 bp 5'
Search 100 bp 3'