ClinGen Allele Registry
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Canonical Allele Identifier:
CA890579932
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1171909053
gnomAD v3:
1-165478767-G-A
gnomAD v4:
1-165478767-G-A
MyVariant Identifiers:
chr1:g.165448004G>A (hg19)
chr1:g.165478767G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478767G>A , CM000663.2:g.165478767G>A
GRCh38
NC_000001.10:g.165448004G>A , CM000663.1:g.165448004G>A
GRCh37
NC_000001.9:g.163714628G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026744.2:n.1530-1652C>T
Search 100 bp 5'
Search 100 bp 3'