Canonical Allele Identifier: CA550489563

Gene: LINC02357

Linked Data

• dbSNP Id: rs1336923041
• gnomAD v2: 4-26085569-C-T
• gnomAD v3: 4-26083947-C-T
• gnomAD v4: 4-26083947-C-T
• MyVariant Identifiers: chr4:g.26085569C>T (hg19) ; chr4:g.26083947C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083947C>T , CM000666.2:g.26083947C>T	GRCh38
NC_000004.11:g.26085569C>T , CM000666.1:g.26085569C>T	GRCh37
NC_000004.10:g.25694667C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_925506.1:n.1401+3357C>T
XR_925506.3:n.1408+3357C>T