Canonical Allele Identifier: CA94354159
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs139021560

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083864_26083865del , CM000666.2:g.26083864_26083865del GRCh38
NC_000004.11:g.26085486_26085487del , CM000666.1:g.26085486_26085487del GRCh37
NC_000004.10:g.25694584_25694585del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3274_1401+3275del
XR_925506.3:n.1408+3274_1408+3275del