ClinGen Allele Registry
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Canonical Allele Identifier:
CA32228024
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs933192623
gnomAD v2:
1-165448057-T-G
gnomAD v3:
1-165478820-T-G
gnomAD v4:
1-165478820-T-G
MyVariant Identifiers:
chr1:g.165448057T>G (hg19)
chr1:g.165478820T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478820T>G , CM000663.2:g.165478820T>G
GRCh38
NC_000001.10:g.165448057T>G , CM000663.1:g.165448057T>G
GRCh37
NC_000001.9:g.163714681T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_026744.2:n.1530-1705A>C
Search 100 bp 5'
Search 100 bp 3'