Canonical Allele Identifier: CA2355189505
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982722279

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069804C>G , CM000682.2:g.22069804C>G GRCh38
NC_000020.10:g.22050442C>G , CM000682.1:g.22050442C>G GRCh37
NC_000020.9:g.21998442C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1116C>G