Canonical Allele Identifier: CA94354156
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs900445997
MyVariant Identifiers: chr4:g.26085462G>A (hg19) chr4:g.26083840G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083840G>A , CM000666.2:g.26083840G>A GRCh38
NC_000004.11:g.26085462G>A , CM000666.1:g.26085462G>A GRCh37
NC_000004.10:g.25694560G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3250G>A
XR_925506.3:n.1408+3250G>A
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