Canonical Allele Identifier: CA528919739

Gene: LINC02775

Linked Data

• dbSNP Id: rs1202184598
• gnomAD v2: 1-214261195-A-G
• gnomAD v3: 1-214087852-A-G
• gnomAD v4: 1-214087852-A-G
• MyVariant Identifiers: chr1:g.214261195A>G (hg19) ; chr1:g.214087852A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087852A>G , CM000663.2:g.214087852A>G	GRCh38
NC_000001.10:g.214261195A>G , CM000663.1:g.214261195A>G	GRCh37
NC_000001.9:g.212327818A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15414T>C	XP_011508605.1:n.-188-15414T>C
XR_922584.1:n.119-15414T>C
XR_922584.2:n.261-15414T>C