Canonical Allele Identifier: CA2607139500
Gene: LINC02775 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087717A>G , CM000663.2:g.214087717A>G GRCh38
NC_000001.10:g.214261060A>G , CM000663.1:g.214261060A>G GRCh37
NC_000001.9:g.212327683A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15279T>C XP_011508605.1:n.-188-15279T>C
XR_922584.1:n.119-15279T>C
XR_922584.2:n.261-15279T>C