Canonical Allele Identifier: CA731228628
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1392293138
gnomAD v3: 1-214087723-CA-C
gnomAD v4: 1-214087723-CA-C
MyVariant Identifiers: chr1:g.214261067del (hg19) chr1:g.214087724del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087726del , CM000663.2:g.214087726del GRCh38
NC_000001.10:g.214261069del , CM000663.1:g.214261069del GRCh37
NC_000001.9:g.212327692del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15286del XP_011508605.1:n.-188-15286del
XR_922584.1:n.119-15286del
XR_922584.2:n.261-15286del
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