Canonical Allele Identifier: CA2760799682
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083991G>C , CM000666.2:g.26083991G>C GRCh38
NC_000004.11:g.26085613G>C , CM000666.1:g.26085613G>C GRCh37
NC_000004.10:g.25694711G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3401G>C
XR_925506.3:n.1408+3401G>C