Canonical Allele Identifier: CA94354176

Gene: LINC02357

Linked Data

• dbSNP Id: rs934700249
• MyVariant Identifiers: chr4:g.26085610G>A (hg19) ; chr4:g.26083988G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083988G>A , CM000666.2:g.26083988G>A	GRCh38
NC_000004.11:g.26085610G>A , CM000666.1:g.26085610G>A	GRCh37
NC_000004.10:g.25694708G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3398G>A
XR_925506.3:n.1408+3398G>A