Canonical Allele Identifier: CA2549621462

Gene: LINC02775

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087736G>T , CM000663.2:g.214087736G>T	GRCh38
NC_000001.10:g.214261079G>T , CM000663.1:g.214261079G>T	GRCh37
NC_000001.9:g.212327702G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15298C>A	XP_011508605.1:n.-188-15298C>A
XR_922584.1:n.119-15298C>A
XR_922584.2:n.261-15298C>A