Canonical Allele Identifier: CA1445661211
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083820C= , CM000666.2:g.26083820C= GRCh38
NC_000004.11:g.26085442C= , CM000666.1:g.26085442C= GRCh37
NC_000004.10:g.25694540C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3230C=
XR_925506.3:n.1408+3230C=