Canonical Allele Identifier: CA1445661249
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714636677

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083862A>G , CM000666.2:g.26083862A>G GRCh38
NC_000004.11:g.26085484A>G , CM000666.1:g.26085484A>G GRCh37
NC_000004.10:g.25694582A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3272A>G
XR_925506.3:n.1408+3272A>G