Canonical Allele Identifier: CA2355189595
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1852712955

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069974T>G , CM000682.2:g.22069974T>G GRCh38
NC_000020.10:g.22050612T>G , CM000682.1:g.22050612T>G GRCh37
NC_000020.9:g.21998612T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1286T>G