Canonical Allele Identifier: CA313071802

Gene: LINC01432

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22061780A>C , CM000682.2:g.22061780A>C	GRCh38
NC_000020.10:g.22042418A>C , CM000682.1:g.22042418A>C	GRCh37
NC_000020.9:g.21990418A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.196-6659A>C