Canonical Allele Identifier: CA2123683198
Gene: LINC00596 HGNC NCBI

Linked Data

dbSNP Id: rs2031834669
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912329G>A , CM000676.2:g.23912329G>A GRCh38
NC_000014.8:g.24381538G>A , CM000676.1:g.24381538G>A GRCh37
NC_000014.7:g.23451378G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_429343.2:n.179-9617C>T
XR_001750659.1:n.196-9617C>T
XR_429343.3:n.196-9617C>T
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