ClinGen Allele Registry
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Canonical Allele Identifier:
CA890579915
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1437008123
gnomAD v3:
1-165478742-T-C
gnomAD v4:
1-165478742-T-C
MyVariant Identifiers:
chr1:g.165447979T>C (hg19)
chr1:g.165478742T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478742T>C , CM000663.2:g.165478742T>C
GRCh38
NC_000001.10:g.165447979T>C , CM000663.1:g.165447979T>C
GRCh37
NC_000001.9:g.163714603T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026744.2:n.1530-1627A>G
Search 100 bp 5'
Search 100 bp 3'