Canonical Allele Identifier: CA13192239
Gene: LINC02621 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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