Canonical Allele Identifier: CA14624368

Gene: LINC01905 LINC03069

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.56050233C>T , CM000680.2:g.56050233C>T	GRCh38
NC_000018.9:g.53717464C>T , CM000680.1:g.53717464C>T	GRCh37
NC_000018.8:g.51868462C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_146510.1:n.165+56C>T (LINC01905)
NR_146511.1:n.165+56C>T (LINC01905)
NR_148972.1:n.1067+5672G>A (LINC03069)