Canonical Allele Identifier: CA635117116
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1309813170
gnomAD v2: 20-22050757-T-TC
gnomAD v3: 20-22070119-T-TC
gnomAD v4: 20-22070119-T-TC
MyVariant Identifiers: chr20:g.22050757_22050758insC (hg19) chr20:g.22070119_22070120insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070119_22070120insC , CM000682.2:g.22070119_22070120insC GRCh38
NC_000020.10:g.22050757_22050758insC , CM000682.1:g.22050757_22050758insC GRCh37
NC_000020.9:g.21998757_21998758insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1431_445+1432insC
Search 100 bp 5'
Search 100 bp 3'