Canonical Allele Identifier: CA527066326
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1482095934
gnomAD v2: 1-165448189-T-A
gnomAD v3: 1-165478952-T-A
gnomAD v4: 1-165478952-T-A
MyVariant Identifiers: chr1:g.165448189T>A (hg19) chr1:g.165478952T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478952T>A , CM000663.2:g.165478952T>A GRCh38
NC_000001.10:g.165448189T>A , CM000663.1:g.165448189T>A GRCh37
NC_000001.9:g.163714813T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026744.2:n.1530-1837A>T
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