Canonical Allele Identifier: CA793384467

Gene: LINC02357

Linked Data

• dbSNP Id: rs1430379757
• gnomAD v3: 4-26083995-G-A
• gnomAD v4: 4-26083995-G-A
• MyVariant Identifiers: chr4:g.26085617G>A (hg19) ; chr4:g.26083995G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083995G>A , CM000666.2:g.26083995G>A	GRCh38
NC_000004.11:g.26085617G>A , CM000666.1:g.26085617G>A	GRCh37
NC_000004.10:g.25694715G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3405G>A
XR_925506.3:n.1408+3405G>A