Canonical Allele Identifier: CA2736614713
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs2122510267

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059271T>G , CM000682.2:g.22059271T>G GRCh38
NC_000020.10:g.22039909T>G , CM000682.1:g.22039909T>G GRCh37
NC_000020.9:g.21987909T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4987T>G