Canonical Allele Identifier: CA1445661298
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714637542

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083896_26083899del , CM000666.2:g.26083896_26083899del GRCh38
NC_000004.11:g.26085518_26085521del , CM000666.1:g.26085518_26085521del GRCh37
NC_000004.10:g.25694616_25694619del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3306_1401+3309del
XR_925506.3:n.1408+3306_1408+3309del