Canonical Allele Identifier: CA2355189588
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982726312

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069960G>C , CM000682.2:g.22069960G>C GRCh38
NC_000020.10:g.22050598G>C , CM000682.1:g.22050598G>C GRCh37
NC_000020.9:g.21998598G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1272G>C