ClinGen Allele Registry
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Canonical Allele Identifier:
CA890579950
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1220837093
MyVariant Identifiers:
chr1:g.165448050A>T (hg19)
chr1:g.165478813A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478813A>T , CM000663.2:g.165478813A>T
GRCh38
NC_000001.10:g.165448050A>T , CM000663.1:g.165448050A>T
GRCh37
NC_000001.9:g.163714674A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026744.2:n.1530-1698T>A
Search 100 bp 5'
Search 100 bp 3'