Canonical Allele Identifier: CA815335975

Gene: LINC01339

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90250292A>T , CM000667.2:g.90250292A>T	GRCh38
NC_000005.9:g.89546109A>T , CM000667.1:g.89546109A>T	GRCh37
NC_000005.8:g.89581865A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120601.1:n.269+10254T>A