Canonical Allele Identifier: CA528919728
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs780777879
gnomAD v2: 1-214261032-T-A
gnomAD v3: 1-214087689-T-A
gnomAD v4: 1-214087689-T-A
MyVariant Identifiers: chr1:g.214261032T>A (hg19) chr1:g.214087689T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087689T>A , CM000663.2:g.214087689T>A GRCh38
NC_000001.10:g.214261032T>A , CM000663.1:g.214261032T>A GRCh37
NC_000001.9:g.212327655T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15251A>T XP_011508605.1:n.-188-15251A>T
XR_922584.1:n.119-15251A>T
XR_922584.2:n.261-15251A>T
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