Canonical Allele Identifier: CA2815543183
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070117T>G , CM000682.2:g.22070117T>G GRCh38
NC_000020.10:g.22050755T>G , CM000682.1:g.22050755T>G GRCh37
NC_000020.9:g.21998755T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1429T>G