Canonical Allele Identifier: CA2355189519
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982722906

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069821C>T , CM000682.2:g.22069821C>T GRCh38
NC_000020.10:g.22050459C>T , CM000682.1:g.22050459C>T GRCh37
NC_000020.9:g.21998459C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1133C>T