ClinGen Allele Registry
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Canonical Allele Identifier:
CA1253945374
Gene: LINC01122
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
6731302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.58606358A>C , CM000664.2:g.58606358A>C
GRCh38
NC_000002.11:g.58833493A>C , CM000664.1:g.58833493A>C
GRCh37
NC_000002.10:g.58686997A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033873.1:n.186-50292A>C
Search 100 bp 5'
Search 100 bp 3'