Canonical Allele Identifier: CA16587445

Gene: LINC01749

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63037684A>G , CM000682.2:g.63037684A>G	GRCh38
NC_000020.10:g.61669036A>G , CM000682.1:g.61669036A>G	GRCh37
NC_000020.9:g.61139481A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033370.1:n.91+28211A>G