Canonical Allele Identifier: CA527066323
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1407504581
gnomAD v2: 1-165448045-T-G
gnomAD v3: 1-165478808-T-G
gnomAD v4: 1-165478808-T-G
MyVariant Identifiers: chr1:g.165448045T>G (hg19) chr1:g.165478808T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478808T>G , CM000663.2:g.165478808T>G GRCh38
NC_000001.10:g.165448045T>G , CM000663.1:g.165448045T>G GRCh37
NC_000001.9:g.163714669T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1693A>C
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