Canonical Allele Identifier: CA527066322
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1475399039
gnomAD v2: 1-165447980-G-A
gnomAD v3: 1-165478743-G-A
gnomAD v4: 1-165478743-G-A
MyVariant Identifiers: chr1:g.165447980G>A (hg19) chr1:g.165478743G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478743G>A , CM000663.2:g.165478743G>A GRCh38
NC_000001.10:g.165447980G>A , CM000663.1:g.165447980G>A GRCh37
NC_000001.9:g.163714604G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1628C>T
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