Canonical Allele Identifier: CA94354162

Gene: LINC02357

Linked Data

• dbSNP Id: rs182014442
• gnomAD v2: 4-26085488-T-A
• gnomAD v3: 4-26083866-T-A
• gnomAD v4: 4-26083866-T-A
• MyVariant Identifiers: chr4:g.26085488T>A (hg19) ; chr4:g.26083866T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083866T>A , CM000666.2:g.26083866T>A	GRCh38
NC_000004.11:g.26085488T>A , CM000666.1:g.26085488T>A	GRCh37
NC_000004.10:g.25694586T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3276T>A
XR_925506.3:n.1408+3276T>A