Canonical Allele Identifier: CA2594568813
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs2109066145
gnomAD v3: 4-26083963-T-A
gnomAD v4: 4-26083963-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083963T>A , CM000666.2:g.26083963T>A GRCh38
NC_000004.11:g.26085585T>A , CM000666.1:g.26085585T>A GRCh37
NC_000004.10:g.25694683T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3373T>A
XR_925506.3:n.1408+3373T>A