Canonical Allele Identifier: CA1445661318
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1463756291

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083906C>A , CM000666.2:g.26083906C>A GRCh38
NC_000004.11:g.26085528C>A , CM000666.1:g.26085528C>A GRCh37
NC_000004.10:g.25694626C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3316C>A
XR_925506.3:n.1408+3316C>A