Canonical Allele Identifier: CA14785319

Gene: LINC01432

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069865A>G , CM000682.2:g.22069865A>G	GRCh38
NC_000020.10:g.22050503A>G , CM000682.1:g.22050503A>G	GRCh37
NC_000020.9:g.21998503A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1177A>G