ClinGen Allele Registry
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Canonical Allele Identifier:
CA1562661392
Gene: LINC01339
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.90250292A= , CM000667.2:g.90250292A=
GRCh38
NC_000005.9:g.89546109A= , CM000667.1:g.89546109A=
GRCh37
NC_000005.8:g.89581865A=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120601.1:n.269+10254T=
Search 100 bp 5'
Search 100 bp 3'