ClinGen Allele Registry
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Canonical Allele Identifier:
CA1839594735
Gene: LINC01239
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22770887A>T , CM000671.2:g.22770887A>T
GRCh38
NC_000009.11:g.22770886A>T , CM000671.1:g.22770886A>T
GRCh37
NC_000009.10:g.22760886A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038977.1:n.524+47457A>T
Search 100 bp 5'
Search 100 bp 3'