ClinGen Allele Registry
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Canonical Allele Identifier:
CA762147063
Gene: LINC01090
HGNC
NCBI
Linked Data
dbSNP:
7582658
MyVariant.info:
GRCh38
chr2:g.188083114A>C
GRCh37
chr2:g.188947841A>C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.188083114A>C , CM000664.2:g.188083114A>C
GRCh38
NC_000002.11:g.188947841A>C , CM000664.1:g.188947841A>C
GRCh37
NC_000002.10:g.188656086A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126396.1:n.381-47403T>G
Search 100 bp 5'
Search 100 bp 3'