Canonical Allele Identifier: CA528919741

Gene: LINC02775

Linked Data

• dbSNP Id: rs1182250472
• gnomAD v2: 1-214261230-A-T
• gnomAD v3: 1-214087887-A-T
• gnomAD v4: 1-214087887-A-T
• MyVariant Identifiers: chr1:g.214261230A>T (hg19) ; chr1:g.214087887A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087887A>T , CM000663.2:g.214087887A>T	GRCh38
NC_000001.10:g.214261230A>T , CM000663.1:g.214261230A>T	GRCh37
NC_000001.9:g.212327853A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15449T>A	XP_011508605.1:n.-188-15449T>A
XR_922584.1:n.119-15449T>A
XR_922584.2:n.261-15449T>A