Canonical Allele Identifier: CA2736614690
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs2122510244

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059250G>T , CM000682.2:g.22059250G>T GRCh38
NC_000020.10:g.22039888G>T , CM000682.1:g.22039888G>T GRCh37
NC_000020.9:g.21987888G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4966G>T