ClinGen Allele Registry
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Canonical Allele Identifier:
CA2198988000
Gene: LINC02351
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.98332898T= , CM000677.2:g.98332898T=
GRCh38
NC_000015.9:g.98876127T= , CM000677.1:g.98876127T=
GRCh37
NC_000015.8:g.96693650T=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_146567.1:n.191-5445A=
Search 100 bp 5'
Search 100 bp 3'