Canonical Allele Identifier: CA1445661420
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26084039A= , CM000666.2:g.26084039A= GRCh38
NC_000004.11:g.26085661A= , CM000666.1:g.26085661A= GRCh37
NC_000004.10:g.25694759A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3449A=
XR_925506.3:n.1408+3449A=