Canonical Allele Identifier: CA1445661358
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1560423551

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083966G>T , CM000666.2:g.26083966G>T GRCh38
NC_000004.11:g.26085588G>T , CM000666.1:g.26085588G>T GRCh37
NC_000004.10:g.25694686G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3376G>T
XR_925506.3:n.1408+3376G>T