Canonical Allele Identifier: CA793384402
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1208449505
gnomAD v3: 4-26083837-G-A
gnomAD v4: 4-26083837-G-A
MyVariant Identifiers: chr4:g.26085459G>A (hg19) chr4:g.26083837G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083837G>A , CM000666.2:g.26083837G>A GRCh38
NC_000004.11:g.26085459G>A , CM000666.1:g.26085459G>A GRCh37
NC_000004.10:g.25694557G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3247G>A
XR_925506.3:n.1408+3247G>A
Search 100 bp 5'
Search 100 bp 3'