ClinGen Allele Registry
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Canonical Allele Identifier:
CA2198987993
Gene: LINC02351
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.98332891A= , CM000677.2:g.98332891A=
GRCh38
NC_000015.9:g.98876120A= , CM000677.1:g.98876120A=
GRCh37
NC_000015.8:g.96693643A=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_146567.1:n.191-5438T=
Search 100 bp 5'
Search 100 bp 3'