Canonical Allele Identifier: CA2581699129
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088007T>G , CM000663.2:g.214088007T>G GRCh38
NC_000001.10:g.214261350T>G , CM000663.1:g.214261350T>G GRCh37
NC_000001.9:g.212327973T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15569A>C XP_011508605.1:n.-188-15569A>C
XR_922584.1:n.119-15569A>C
XR_922584.2:n.261-15569A>C