Canonical Allele Identifier: CA2123683185
Gene: LINC00596 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912312T= , CM000676.2:g.23912312T= GRCh38
NC_000014.8:g.24381521T= , CM000676.1:g.24381521T= GRCh37
NC_000014.7:g.23451361T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_429343.2:n.179-9600A=
XR_001750659.1:n.196-9600A=
XR_429343.3:n.196-9600A=