Canonical Allele Identifier: CA68900705

Gene: LINC01266

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.842168G>A , CM000665.2:g.842168G>A	GRCh38
NC_000003.11:g.883851G>A , CM000665.1:g.883851G>A	GRCh37
NC_000003.10:g.858851G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110118.1:n.212-208G>A