Canonical Allele Identifier: CA2760799684
Gene: LINC02357 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26084002A>T , CM000666.2:g.26084002A>T GRCh38
NC_000004.11:g.26085624A>T , CM000666.1:g.26085624A>T GRCh37
NC_000004.10:g.25694722A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3412A>T
XR_925506.3:n.1408+3412A>T
Search 100 bp 5'
Search 100 bp 3'