Canonical Allele Identifier: CA793384465

Gene: LINC02357

Linked Data

• dbSNP Id: rs1357313327
• MyVariant Identifiers: chr4:g.26085611A>G (hg19) ; chr4:g.26083989A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083989A>G , CM000666.2:g.26083989A>G	GRCh38
NC_000004.11:g.26085611A>G , CM000666.1:g.26085611A>G	GRCh37
NC_000004.10:g.25694709A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3399A>G
XR_925506.3:n.1408+3399A>G