Canonical Allele Identifier: CA2355189491
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982721480

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069775A>G , CM000682.2:g.22069775A>G GRCh38
NC_000020.10:g.22050413A>G , CM000682.1:g.22050413A>G GRCh37
NC_000020.9:g.21998413A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1087A>G