Canonical Allele Identifier: CA37393248

Gene: LINC02775

Linked Data

• dbSNP Id: rs1035024324
• MyVariant Identifiers: chr1:g.214261144C>A (hg19) ; chr1:g.214087801C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087801C>A , CM000663.2:g.214087801C>A	GRCh38
NC_000001.10:g.214261144C>A , CM000663.1:g.214261144C>A	GRCh37
NC_000001.9:g.212327767C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15363G>T	XP_011508605.1:n.-188-15363G>T
XR_922584.1:n.119-15363G>T
XR_922584.2:n.261-15363G>T