ClinGen Allele Registry
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Canonical Allele Identifier:
CA1791698879
Gene: LINC01592
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.69080145G= , CM000670.2:g.69080145G=
GRCh38
NC_000008.10:g.69992380G= , CM000670.1:g.69992380G=
GRCh37
NC_000008.9:g.70154934G=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_039986.1:n.194-11596C=
Search 100 bp 5'
Search 100 bp 3'