ClinGen Allele Registry
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Canonical Allele Identifier:
CA1763768665
Gene: LINC00529
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11261528C= , CM000670.2:g.11261528C=
GRCh38
NC_000008.10:g.11119037C= , CM000670.1:g.11119037C=
GRCh37
NC_000008.9:g.11156447C=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_170283.1:n.558+6261G=
Search 100 bp 5'
Search 100 bp 3'