Canonical Allele Identifier: CA550489539
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1437067754
gnomAD v2: 4-26085470-A-T
gnomAD v3: 4-26083848-A-T
gnomAD v4: 4-26083848-A-T
MyVariant Identifiers: chr4:g.26085470A>T (hg19) chr4:g.26083848A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083848A>T , CM000666.2:g.26083848A>T GRCh38
NC_000004.11:g.26085470A>T , CM000666.1:g.26085470A>T GRCh37
NC_000004.10:g.25694568A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3258A>T
XR_925506.3:n.1408+3258A>T
Search 100 bp 5'
Search 100 bp 3'