Canonical Allele Identifier: CA1791698878

Gene: LINC01592

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.69080145G>T , CM000670.2:g.69080145G>T	GRCh38
NC_000008.10:g.69992380G>T , CM000670.1:g.69992380G>T	GRCh37
NC_000008.9:g.70154934G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_039986.1:n.194-11596C>A