Canonical Allele Identifier: CA2355189641
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982728557

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070062C>T , CM000682.2:g.22070062C>T GRCh38
NC_000020.10:g.22050700C>T , CM000682.1:g.22050700C>T GRCh37
NC_000020.9:g.21998700C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1374C>T