ClinGen Allele Registry
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Canonical Allele Identifier:
CA1140146863
Gene: LINC01725
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.83789052G= , CM000663.2:g.83789052G=
GRCh38
NC_000001.10:g.84254735G= , CM000663.1:g.84254735G=
GRCh37
NC_000001.9:g.84027323G=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_119375.1:n.179-38753C=
Search 100 bp 5'
Search 100 bp 3'