Canonical Allele Identifier: CA295998618

Gene: LINC01255

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11494200T>C , CM000680.2:g.11494200T>C	GRCh38
NC_000018.9:g.11494199T>C , CM000680.1:g.11494199T>C	GRCh37
NC_000018.8:g.11484199T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110778.1:n.194+3959T>C
NR_110779.1:n.115+5278T>C