Canonical Allele Identifier: CA2355189480
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982720962

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069759G>C , CM000682.2:g.22069759G>C GRCh38
NC_000020.10:g.22050397G>C , CM000682.1:g.22050397G>C GRCh37
NC_000020.9:g.21998397G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1071G>C