ClinGen Allele Registry
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Canonical Allele Identifier:
CA890579967
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1281170019
gnomAD v3:
1-165478863-A-G
gnomAD v4:
1-165478863-A-G
MyVariant Identifiers:
chr1:g.165448100A>G (hg19)
chr1:g.165478863A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478863A>G , CM000663.2:g.165478863A>G
GRCh38
NC_000001.10:g.165448100A>G , CM000663.1:g.165448100A>G
GRCh37
NC_000001.9:g.163714724A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_026744.2:n.1530-1748T>C
Search 100 bp 5'
Search 100 bp 3'