Canonical Allele Identifier: CA2486143485
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1558205859
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087756A>G , CM000663.2:g.214087756A>G GRCh38
NC_000001.10:g.214261099A>G , CM000663.1:g.214261099A>G GRCh37
NC_000001.9:g.212327722A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15318T>C XP_011508605.1:n.-188-15318T>C
XR_922584.1:n.119-15318T>C
XR_922584.2:n.261-15318T>C
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