Canonical Allele Identifier: CA1139874386
Gene: LINC02775 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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