Canonical Allele Identifier: CA793384393

Gene: LINC02357

Linked Data

• dbSNP Id: rs1219555272
• MyVariant Identifiers: chr4:g.26085413_26085423del (hg19) ; chr4:g.26083791_26083801del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083793_26083803del , CM000666.2:g.26083793_26083803del	GRCh38
NC_000004.11:g.26085415_26085425del , CM000666.1:g.26085415_26085425del	GRCh37
NC_000004.10:g.25694513_25694523del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3203_1401+3213del
XR_925506.3:n.1408+3203_1408+3213del