Canonical Allele Identifier: CA1445661364
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714639130

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083978A>C , CM000666.2:g.26083978A>C GRCh38
NC_000004.11:g.26085600A>C , CM000666.1:g.26085600A>C GRCh37
NC_000004.10:g.25694698A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3388A>C
XR_925506.3:n.1408+3388A>C