Canonical Allele Identifier: CA313071222

Gene: LINC01432

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22056937T>C , CM000682.2:g.22056937T>C	GRCh38
NC_000020.10:g.22037575T>C , CM000682.1:g.22037575T>C	GRCh37
NC_000020.9:g.21985575T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.195+2653T>C