Canonical Allele Identifier: CA1445661303
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714637578

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083900_26083901insGG , CM000666.2:g.26083900_26083901insGG GRCh38
NC_000004.11:g.26085522_26085523insGG , CM000666.1:g.26085522_26085523insGG GRCh37
NC_000004.10:g.25694620_25694621insGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3310_1401+3311insGG
XR_925506.3:n.1408+3310_1408+3311insGG