Canonical Allele Identifier: CA731228693

Gene: LINC02775

Linked Data

• dbSNP Id: rs1283447000
• gnomAD v3: 1-214087883-C-T
• gnomAD v4: 1-214087883-C-T
• MyVariant Identifiers: chr1:g.214261226C>T (hg19) ; chr1:g.214087883C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087883C>T , CM000663.2:g.214087883C>T	GRCh38
NC_000001.10:g.214261226C>T , CM000663.1:g.214261226C>T	GRCh37
NC_000001.9:g.212327849C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15445G>A	XP_011508605.1:n.-188-15445G>A
XR_922584.1:n.119-15445G>A
XR_922584.2:n.261-15445G>A