Canonical Allele Identifier: CA1445661267
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714636936

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083871A>G , CM000666.2:g.26083871A>G GRCh38
NC_000004.11:g.26085493A>G , CM000666.1:g.26085493A>G GRCh37
NC_000004.10:g.25694591A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3281A>G
XR_925506.3:n.1408+3281A>G