Canonical Allele Identifier: CA2815543174
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070108A>C , CM000682.2:g.22070108A>C GRCh38
NC_000020.10:g.22050746A>C , CM000682.1:g.22050746A>C GRCh37
NC_000020.9:g.21998746A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1420A>C