Canonical Allele Identifier: CA2705535969
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs2109066153

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083993G>A , CM000666.2:g.26083993G>A GRCh38
NC_000004.11:g.26085615G>A , CM000666.1:g.26085615G>A GRCh37
NC_000004.10:g.25694713G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3403G>A
XR_925506.3:n.1408+3403G>A