Canonical Allele Identifier: CA2838144234
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083858A>T , CM000666.2:g.26083858A>T GRCh38
NC_000004.11:g.26085480A>T , CM000666.1:g.26085480A>T GRCh37
NC_000004.10:g.25694578A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3268A>T
XR_925506.3:n.1408+3268A>T