Canonical Allele Identifier: CA324925153

Gene: LINC00229

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.44615881G>C , CM000684.2:g.44615881G>C	GRCh38
NC_000022.10:g.45011761G>C , CM000684.1:g.45011761G>C	GRCh37
NC_000022.9:g.43390425G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_044991.1:n.390+6406C>G