Canonical Allele Identifier: CA793384428

Gene: LINC02357

Linked Data

• dbSNP Id: rs139021560
• MyVariant Identifiers: chr4:g.26085476_26085479del (hg19) ; chr4:g.26083854_26083857del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083862_26083865del , CM000666.2:g.26083862_26083865del	GRCh38
NC_000004.11:g.26085484_26085487del , CM000666.1:g.26085484_26085487del	GRCh37
NC_000004.10:g.25694582_25694585del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3272_1401+3275del
XR_925506.3:n.1408+3272_1408+3275del