Canonical Allele Identifier: CA2355189639
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982728482

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070060C>T , CM000682.2:g.22070060C>T GRCh38
NC_000020.10:g.22050698C>T , CM000682.1:g.22050698C>T GRCh37
NC_000020.9:g.21998698C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1372C>T