Canonical Allele Identifier: CA11881937

Gene: LINC02357

Linked Data

• dbSNP Id: rs34185821
• gnomAD v2: 4-26085480-A-G
• gnomAD v3: 4-26083858-A-G
• gnomAD v4: 4-26083858-A-G
• MyVariant Identifiers: chr4:g.26085480A>G (hg19) ; chr4:g.26083858A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083858A>G , CM000666.2:g.26083858A>G	GRCh38
NC_000004.11:g.26085480A>G , CM000666.1:g.26085480A>G	GRCh37
NC_000004.10:g.25694578A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3268A>G
XR_925506.3:n.1408+3268A>G