Canonical Allele Identifier: CA1016142433
Gene: LINC01432 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070132T>C , CM000682.2:g.22070132T>C GRCh38
NC_000020.10:g.22050770T>C , CM000682.1:g.22050770T>C GRCh37
NC_000020.9:g.21998770T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1444T>C