Canonical Allele Identifier: CA94354173
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs144229942

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083929_26083931del , CM000666.2:g.26083929_26083931del GRCh38
NC_000004.11:g.26085551_26085553del , CM000666.1:g.26085551_26085553del GRCh37
NC_000004.10:g.25694649_25694651del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3339_1401+3341del
XR_925506.3:n.1408+3339_1408+3341del