Canonical Allele Identifier: CA528919721
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1444569228
gnomAD v2: 1-214261011-CTTTA-C
gnomAD v3: 1-214087668-CTTTA-C
gnomAD v4: 1-214087668-CTTTA-C
MyVariant Identifiers: chr1:g.214261012_214261015del (hg19) chr1:g.214087669_214087672del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087674_214087677del , CM000663.2:g.214087674_214087677del GRCh38
NC_000001.10:g.214261017_214261020del , CM000663.1:g.214261017_214261020del GRCh37
NC_000001.9:g.212327640_212327643del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15234_-188-15231del XP_011508605.1:n.-188-15234_-188-15231del
XR_922584.1:n.119-15234_119-15231del
XR_922584.2:n.261-15234_261-15231del
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