Canonical Allele Identifier: CA1445661389
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26084013C= , CM000666.2:g.26084013C= GRCh38
NC_000004.11:g.26085635C= , CM000666.1:g.26085635C= GRCh37
NC_000004.10:g.25694733C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3423C=
XR_925506.3:n.1408+3423C=