Canonical Allele Identifier: CA37393253

Gene: LINC02775

Linked Data

• dbSNP Id: rs184627221
• gnomAD v3: 1-214087824-G-C
• gnomAD v4: 1-214087824-G-C
• MyVariant Identifiers: chr1:g.214261167G>C (hg19) ; chr1:g.214087824G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087824G>C , CM000663.2:g.214087824G>C	GRCh38
NC_000001.10:g.214261167G>C , CM000663.1:g.214261167G>C	GRCh37
NC_000001.9:g.212327790G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15386C>G	XP_011508605.1:n.-188-15386C>G
XR_922584.1:n.119-15386C>G
XR_922584.2:n.261-15386C>G