ClinGen Allele Registry
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Canonical Allele Identifier:
CA527066320
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1190325553
gnomAD v2:
1-165447966-A-T
gnomAD v3:
1-165478729-A-T
gnomAD v4:
1-165478729-A-T
MyVariant Identifiers:
chr1:g.165447966A>T (hg19)
chr1:g.165478729A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478729A>T , CM000663.2:g.165478729A>T
GRCh38
NC_000001.10:g.165447966A>T , CM000663.1:g.165447966A>T
GRCh37
NC_000001.9:g.163714590A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026744.2:n.1530-1614T>A
Search 100 bp 5'
Search 100 bp 3'