Canonical Allele Identifier: CA594026357
Gene: LINC02621 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62277122G>T , CM000672.2:g.62277122G>T GRCh38
NC_000010.10:g.64036881G>T , CM000672.1:g.64036881G>T GRCh37
NC_000010.9:g.63706887G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945999.1:n.125-25204G>T