Canonical Allele Identifier: CA1016142591
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070157-A-C
gnomAD v4: 20-22070157-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070157A>C , CM000682.2:g.22070157A>C GRCh38
NC_000020.10:g.22050795A>C , CM000682.1:g.22050795A>C GRCh37
NC_000020.9:g.21998795A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1469A>C
Search 100 bp 5'
Search 100 bp 3'