ClinGen Allele Registry
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Canonical Allele Identifier:
CA1254061506
Gene: LINC01122
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.58845834C= , CM000664.2:g.58845834C=
GRCh38
NC_000002.11:g.59072969C= , CM000664.1:g.59072969C=
GRCh37
NC_000002.10:g.58926473C=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033873.1:n.248-4596C=
Search 100 bp 5'
Search 100 bp 3'