ClinGen Allele Registry
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Canonical Allele Identifier:
CA1470816780
Gene: LINC01088
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.79043433A= , CM000666.2:g.79043433A=
GRCh38
NC_000004.11:g.79964587A= , CM000666.1:g.79964587A=
GRCh37
NC_000004.10:g.80183611A=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038342.1:n.183-42663A=
Search 100 bp 5'
Search 100 bp 3'