Canonical Allele Identifier: CA2355189666
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs962639336

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070110C>G , CM000682.2:g.22070110C>G GRCh38
NC_000020.10:g.22050748C>G , CM000682.1:g.22050748C>G GRCh37
NC_000020.9:g.21998748C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1422C>G