ClinGen Allele Registry
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Canonical Allele Identifier:
CA1254163837
Gene: LINC01122
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
991964
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.59055456T>G , CM000664.2:g.59055456T>G
GRCh38
NC_000002.11:g.59282591T>G , CM000664.1:g.59282591T>G
GRCh37
NC_000002.10:g.59136095T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033873.1:n.1273-3105T>G
Search 100 bp 5'
Search 100 bp 3'