Canonical Allele Identifier: CA1888181352
Gene: LINC02656 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6348488G>T , CM000672.2:g.6348488G>T GRCh38
NC_000010.10:g.6390450G>T , CM000672.1:g.6390450G>T GRCh37
NC_000010.9:g.6430456G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_242715.2:n.1306G>T