Canonical Allele Identifier: CA2594568814
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs2109066146
gnomAD v3: 4-26083964-C-T
gnomAD v4: 4-26083964-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083964C>T , CM000666.2:g.26083964C>T GRCh38
NC_000004.11:g.26085586C>T , CM000666.1:g.26085586C>T GRCh37
NC_000004.10:g.25694684C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3374C>T
XR_925506.3:n.1408+3374C>T