Canonical Allele Identifier: CA37393549

Gene: LINC02775

Linked Data

• dbSNP Id: rs551347310
• gnomAD v3: 1-214088035-T-C
• gnomAD v4: 1-214088035-T-C
• MyVariant Identifiers: chr1:g.214261378T>C (hg19) ; chr1:g.214088035T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214088035T>C , CM000663.2:g.214088035T>C	GRCh38
NC_000001.10:g.214261378T>C , CM000663.1:g.214261378T>C	GRCh37
NC_000001.9:g.212328001T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15597A>G	XP_011508605.1:n.-188-15597A>G
XR_922584.1:n.119-15597A>G
XR_922584.2:n.261-15597A>G