Canonical Allele Identifier: CA15326042
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26097188G>A , CM000666.2:g.26097188G>A GRCh38
NC_000004.11:g.26098810G>A , CM000666.1:g.26098810G>A GRCh37
NC_000004.10:g.25707908G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1402-6857G>A
XR_925506.3:n.1409-6857G>A