Canonical Allele Identifier: CA793384447

Gene: LINC02357

Linked Data

• dbSNP Id: rs1463756291
• gnomAD v3: 4-26083906-C-T
• gnomAD v4: 4-26083906-C-T
• MyVariant Identifiers: chr4:g.26085528C>T (hg19) ; chr4:g.26083906C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083906C>T , CM000666.2:g.26083906C>T	GRCh38
NC_000004.11:g.26085528C>T , CM000666.1:g.26085528C>T	GRCh37
NC_000004.10:g.25694626C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3316C>T
XR_925506.3:n.1408+3316C>T