Canonical Allele Identifier: CA94354158
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs139021560
gnomAD v2: 4-26085475-C-CAT
gnomAD v3: 4-26083853-C-CAT
gnomAD v4: 4-26083853-C-CAT
MyVariant Identifiers: chr4:g.26085477_26085478insAT (hg19) chr4:g.26085475_26085476insAT (hg19) chr4:g.26083855_26083856insAT (hg38) chr4:g.26083853_26083854insAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083864_26083865dup , CM000666.2:g.26083864_26083865dup GRCh38
NC_000004.11:g.26085486_26085487dup , CM000666.1:g.26085486_26085487dup GRCh37
NC_000004.10:g.25694584_25694585dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3274_1401+3275dup
XR_925506.3:n.1408+3274_1408+3275dup
Search 100 bp 5'
Search 100 bp 3'