Canonical Allele Identifier: CA2560386610
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083873A>C , CM000666.2:g.26083873A>C GRCh38
NC_000004.11:g.26085495A>C , CM000666.1:g.26085495A>C GRCh37
NC_000004.10:g.25694593A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3283A>C
XR_925506.3:n.1408+3283A>C