Canonical Allele Identifier: CA2736614201
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs2122520436

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069681A>T , CM000682.2:g.22069681A>T GRCh38
NC_000020.10:g.22050319A>T , CM000682.1:g.22050319A>T GRCh37
NC_000020.9:g.21998319A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+993A>T