Canonical Allele Identifier: CA1445661209
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714635278

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083819C>A , CM000666.2:g.26083819C>A GRCh38
NC_000004.11:g.26085441C>A , CM000666.1:g.26085441C>A GRCh37
NC_000004.10:g.25694539C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3229C>A
XR_925506.3:n.1408+3229C>A